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MondoRelease_2020-12-018.txt
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MondoRelease_2020-12-018.txt
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## New Classes
* [MONDO:0020836](http://purl.obolibrary.org/obo/MONDO_0020836) autism, susceptiblity to
* [MONDO:0026771](http://purl.obolibrary.org/obo/MONDO_0026771) developmental and epileptic encephalopathy, 85, with or without midline brain defects
* [MONDO:0026777](http://purl.obolibrary.org/obo/MONDO_0026777) VEXAS syndrome
* [MONDO:0033613](http://purl.obolibrary.org/obo/MONDO_0033613) neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
* [MONDO:0033614](http://purl.obolibrary.org/obo/MONDO_0033614) spastic paraplegia 83, autosomal recessive
* [MONDO:0033615](http://purl.obolibrary.org/obo/MONDO_0033615) coenzyme q10 deficiency, primary, 9
* [MONDO:0033618](http://purl.obolibrary.org/obo/MONDO_0033618) Vissers-Bodmer syndrome
* [MONDO:0033619](http://purl.obolibrary.org/obo/MONDO_0033619) myopathy, epilepsy, and progressive cerebral atrophy
* [MONDO:0033620](http://purl.obolibrary.org/obo/MONDO_0033620) myofibrillar myopathy 10
* [MONDO:0033621](http://purl.obolibrary.org/obo/MONDO_0033621) spinal muscular atrophy, infantile, James type
* [MONDO:0033622](http://purl.obolibrary.org/obo/MONDO_0033622) spermatogenic failure 44
* [MONDO:0033630](http://purl.obolibrary.org/obo/MONDO_0033630) neurodevelopmental disorder with speech impairment and dysmorphic facies
* [MONDO:0033631](http://purl.obolibrary.org/obo/MONDO_0033631) combined oxidative phosphorylation deficiency 51
* [MONDO:0033635](http://purl.obolibrary.org/obo/MONDO_0033635) mitochondrial complex 4 deficiency, nuclear type 3
* [MONDO:0033636](http://purl.obolibrary.org/obo/MONDO_0033636) mitochondrial complex 4 deficiency, nuclear type 4
* [MONDO:0033637](http://purl.obolibrary.org/obo/MONDO_0033637) mitochondrial complex 4 deficiency, nuclear type 7
* [MONDO:0033638](http://purl.obolibrary.org/obo/MONDO_0033638) mitochondrial complex 4 deficiency, nuclear type 8
* [MONDO:0033639](http://purl.obolibrary.org/obo/MONDO_0033639) mitochondrial complex 4 deficiency, nuclear type 10
* [MONDO:0033640](http://purl.obolibrary.org/obo/MONDO_0033640) vitamin D-dependent rickets, type 3
* [MONDO:0033641](http://purl.obolibrary.org/obo/MONDO_0033641) cleft palate, proliferative retinopathy, and developmental delay
* [MONDO:0033642](http://purl.obolibrary.org/obo/MONDO_0033642) neurodevelopmental disorder with alopecia and brain abnormalities
* [MONDO:0033643](http://purl.obolibrary.org/obo/MONDO_0033643) inflammatory bowel disease 30
* [MONDO:0033644](http://purl.obolibrary.org/obo/MONDO_0033644) microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1
* [MONDO:0033645](http://purl.obolibrary.org/obo/MONDO_0033645) mitochondrial complex 4 deficiency, nuclear type 11
* [MONDO:0033646](http://purl.obolibrary.org/obo/MONDO_0033646) mitochondrial complex 4 deficiency, nuclear type 12
* [MONDO:0033649](http://purl.obolibrary.org/obo/MONDO_0033649) mitochondrial complex 4 deficiency, nuclear type 14
* [MONDO:0033650](http://purl.obolibrary.org/obo/MONDO_0033650) mitochondrial complex 4 deficiency, nuclear type 15
* [MONDO:0033651](http://purl.obolibrary.org/obo/MONDO_0033651) mitochondrial complex 4 deficiency, nuclear type 16
* [MONDO:0033652](http://purl.obolibrary.org/obo/MONDO_0033652) mitochondrial complex 4 deficiency, nuclear type 17
* [MONDO:0033653](http://purl.obolibrary.org/obo/MONDO_0033653) mitochondrial complex 4 deficiency, nuclear type 18
* [MONDO:0033654](http://purl.obolibrary.org/obo/MONDO_0033654) mitochondrial complex 4 deficiency, nuclear type 19
* [MONDO:0033655](http://purl.obolibrary.org/obo/MONDO_0033655) mitochondrial complex 4 deficiency, nuclear type 20
* [MONDO:0033656](http://purl.obolibrary.org/obo/MONDO_0033656) mitochondrial complex 4 deficiency, nuclear type 21
* [MONDO:0033657](http://purl.obolibrary.org/obo/MONDO_0033657) leukodystrophy, hypomyelinating, 20
* [MONDO:0033658](http://purl.obolibrary.org/obo/MONDO_0033658) neurodevelopmental disorder with seizures and brain atrophy
* [MONDO:0033662](http://purl.obolibrary.org/obo/MONDO_0033662) neurodevelopmental disorder with microcephaly, seizures, and brain atrophy
* [MONDO:0033664](http://purl.obolibrary.org/obo/MONDO_0033664) Kilquist syndrome
* [MONDO:0033665](http://purl.obolibrary.org/obo/MONDO_0033665) deafness, autosomal dominant 78
* [MONDO:0033667](http://purl.obolibrary.org/obo/MONDO_0033667) Delpire-McNeill syndrome
* [MONDO:0033668](http://purl.obolibrary.org/obo/MONDO_0033668) deafness, autosomal dominant 79
* [MONDO:0033669](http://purl.obolibrary.org/obo/MONDO_0033669) Noonan syndrome 13
* [MONDO:0033670](http://purl.obolibrary.org/obo/MONDO_0033670) deafness, autosomal recessive 116
* [MONDO:0033671](http://purl.obolibrary.org/obo/MONDO_0033671) spermatogenic failure 45
* [MONDO:0033673](http://purl.obolibrary.org/obo/MONDO_0033673) spermatogenic failure 46
* [MONDO:0033885](http://purl.obolibrary.org/obo/MONDO_0033885) mitochondrial complex IV deficiency, nuclear-type
* [MONDO:0034846](http://purl.obolibrary.org/obo/MONDO_0034846) primary desmosis coli
* [MONDO:0034976](http://purl.obolibrary.org/obo/MONDO_0034976) iatrogenic Creutzfeldt-Jakob disease
* [MONDO:0034987](http://purl.obolibrary.org/obo/MONDO_0034987) intraductal tubulopapillary neoplasm of pancreas
* [MONDO:0035004](http://purl.obolibrary.org/obo/MONDO_0035004) serine biosynthesis pathway deficiency, infantile/juvenile form
* [MONDO:0035008](http://purl.obolibrary.org/obo/MONDO_0035008) isolated splenic vein thrombosis
* [MONDO:0035009](http://purl.obolibrary.org/obo/MONDO_0035009) isolated mesenteric vein thrombosis
* [MONDO:0100195](http://purl.obolibrary.org/obo/MONDO_0100195) X-linked intellectual disability with hypopituitarism
* [MONDO:0100222](http://purl.obolibrary.org/obo/MONDO_0100222) A20 haploinsufficiency
* [MONDO:0100223](http://purl.obolibrary.org/obo/MONDO_0100223) mitochondrial complex I deficiency, nuclear type
* [MONDO:0100224](http://purl.obolibrary.org/obo/MONDO_0100224) mitochondrial complex I deficiency, nuclear type 1
* [MONDO:0100225](http://purl.obolibrary.org/obo/MONDO_0100225) collagen 6-related myopathy
* [MONDO:0100226](http://purl.obolibrary.org/obo/MONDO_0100226) parasomnia, sleepwalking type
## Obsoletions
* [MONDO:0000049](http://purl.obolibrary.org/obo/MONDO_0000049) invasive pneumococcal disease, recurrent isolated --> obsolete invasive pneumococcal disease, recurrent isolated
* [MONDO:0000123](http://purl.obolibrary.org/obo/MONDO_0000123) obsolete factor v and Factor VIII, combined deficiency of --> obsolete factor V and Factor VIII, combined deficiency of
* [MONDO:0001807](http://purl.obolibrary.org/obo/MONDO_0001807) familial combined hyperlipidemia --> obsolete familial combined hyperlipidemia
* [MONDO:0001932](http://purl.obolibrary.org/obo/MONDO_0001932) atrophic vulva --> obsolete atrophic vulva
* [MONDO:0002264](http://purl.obolibrary.org/obo/MONDO_0002264) atrophy of prostate --> obsolete atrophy of prostate
* [MONDO:0006168](http://purl.obolibrary.org/obo/MONDO_0006168) common hematopoietic neoplasm --> obsolete common hematopoietic neoplasm
* [MONDO:0006315](http://purl.obolibrary.org/obo/MONDO_0006315) neoplastic medium-sized B-lymphocyte with basophilic cytoplasm --> obsolete neoplastic medium-sized B-lymphocyte with basophilic cytoplasm
* [MONDO:0007347](http://purl.obolibrary.org/obo/MONDO_0007347) CXB3S --> obsolete Coxsackievirus B3 susceptibility
* [MONDO:0007468](http://purl.obolibrary.org/obo/MONDO_0007468) DNA, satellite, alpha type --> obsolete DNA, satellite, alpha type
* [MONDO:0007506](http://purl.obolibrary.org/obo/MONDO_0007506) echo virus 11 sensitivity --> obsoleted echo virus 11 sensitivity
* [MONDO:0008657](http://purl.obolibrary.org/obo/MONDO_0008657) vibratory angioedema --> obsolete vibratory angioedema
* [MONDO:0008761](http://purl.obolibrary.org/obo/MONDO_0008761) alpha-2-deficient collagen disease --> obsolete alpha-2-deficient collagen disease
* [MONDO:0009304](http://purl.obolibrary.org/obo/MONDO_0009304) Gorlin-Chaudhry-Moss syndrome --> obsolete Gorlin-Chaudhry-Moss syndrome
* [MONDO:0009640](http://purl.obolibrary.org/obo/MONDO_0009640) mitochondrial complex I deficiency, nuclear type --> obsolete mitochondrial complex I deficiency, nuclear type
* [MONDO:0010071](http://purl.obolibrary.org/obo/MONDO_0010071) spondyloenchondrodysplasia --> obsolete spondyloenchondrodysplasia
* [MONDO:0010195](http://purl.obolibrary.org/obo/MONDO_0010195) Weissenbacher-Zweymuller syndrome --> obsolete Weissenbacher-Zweymuller syndrome
* [MONDO:0010272](http://purl.obolibrary.org/obo/MONDO_0010272) syndromic X-linked intellectual disability type 10 --> obsolete syndromic X-linked intellectual disability type 10
* [MONDO:0010357](http://purl.obolibrary.org/obo/MONDO_0010357) MRX78 --> obsolete MRX78
* [MONDO:0010376](http://purl.obolibrary.org/obo/MONDO_0010376) Brooks-Wisniewski-brown syndrome --> obsolete Brooks-Wisniewski-brown syndrome
* [MONDO:0010387](http://purl.obolibrary.org/obo/MONDO_0010387) invasive pneumococcal disease, recurrent isolated, 2 --> obsolete invasive pneumococcal disease, recurrent isolated, 2
* [MONDO:0011324](http://purl.obolibrary.org/obo/MONDO_0011324) hypospadias, hypertelorism, upper 51D coloboma, and mixed-type hearing loss --> obsolete hypospadias, hypertelorism, upper 51D coloboma, and mixed-type hearing loss
* [MONDO:0011859](http://purl.obolibrary.org/obo/MONDO_0011859) distal myopathy with early respiratory muscle involvement --> obsolete distal myopathy with early respiratory muscle involvement
* [MONDO:0012189](http://purl.obolibrary.org/obo/MONDO_0012189) Amish infantile epilepsy syndrome --> obsolete Amish infantile epilepsy syndrome
* [MONDO:0012560](http://purl.obolibrary.org/obo/MONDO_0012560) invasive pneumococcal disease, recurrent isolated, 1 --> obsolete invasive pneumococcal disease, recurrent isolated, 1
* [MONDO:0013494](http://purl.obolibrary.org/obo/MONDO_0013494) PSMNSW --> obsolete PSMNSW
* [MONDO:0013701](http://purl.obolibrary.org/obo/MONDO_0013701) MRT32 --> obsolete MRT32
* [MONDO:0015172](http://purl.obolibrary.org/obo/MONDO_0015172) epithelio-exfoliative colitis-deafness syndrome --> obsolete epithelio-exfoliative colitis-deafness syndrome
* [MONDO:0015173](http://purl.obolibrary.org/obo/MONDO_0015173) autoimmune enteropathy type 2 --> obsolete autoimmune enteropathy type 2
* [MONDO:0015297](http://purl.obolibrary.org/obo/MONDO_0015297) microcephaly-digital anomalies-intellectual disability syndrome --> obsolete microcephaly-digital anomalies-intellectual disability syndrome
* [MONDO:0015560](http://purl.obolibrary.org/obo/MONDO_0015560) classic mast cell leukemia --> obsolete classic mast cell leukemia
* [MONDO:0015602](http://purl.obolibrary.org/obo/MONDO_0015602) developmental delay-deafness syndrome, Hildebrand type --> obsolete developmental delay-deafness syndrome, Hildebrand type
* [MONDO:0015964](http://purl.obolibrary.org/obo/MONDO_0015964) rare genetic palpebral, lacrimal system and conjunctival disease --> obsolete rare genetic palpebral, lacrimal system and conjunctival disease
* [MONDO:0016082](http://purl.obolibrary.org/obo/MONDO_0016082) tracheo-esophageal fistula-hypospadias syndrome --> obsolete tracheo-esophageal fistula-hypospadias syndrome
* [MONDO:0016111](http://purl.obolibrary.org/obo/MONDO_0016111) non-dystrophic myopathy with collagen 6 anomaly --> obsolete non-dystrophic myopathy with collagen 6 anomaly
* [MONDO:0016124](http://purl.obolibrary.org/obo/MONDO_0016124) drug and/or toxic myopathy --> obsolete drug and/or toxic myopathy
* [MONDO:0016997](http://purl.obolibrary.org/obo/MONDO_0016997) hereditary epidermolysis bullosa associated with ocular features --> obsolete hereditary epidermolysis bullosa associated with ocular features
* [MONDO:0017378](http://purl.obolibrary.org/obo/MONDO_0017378) polymicrogyria-turricephaly-hypogenitalism syndrome --> obsolete polymicrogyria-turricephaly-hypogenitalism syndrome
* [MONDO:0017458](http://purl.obolibrary.org/obo/MONDO_0017458) postaxial polydactyly of toes --> obsolete postaxial polydactyly of toes
* [MONDO:0017459](http://purl.obolibrary.org/obo/MONDO_0017459) central polydactyly of toes --> obsolete central polydactyly of toes
* [MONDO:0017494](http://purl.obolibrary.org/obo/MONDO_0017494) congenital absence of upper arm and forearm with hand present, unilateral --> obsolete congenital absence of upper arm and forearm with hand present, unilateral
* [MONDO:0017495](http://purl.obolibrary.org/obo/MONDO_0017495) congenital absence of upper arm and forearm with hand present, bilateral --> obsolete congenital absence of upper arm and forearm with hand present, bilateral
* [MONDO:0017539](http://purl.obolibrary.org/obo/MONDO_0017539) postaxial polydactyly of toes, unilateral --> obsolete postaxial polydactyly of toes, unilateral
* [MONDO:0017540](http://purl.obolibrary.org/obo/MONDO_0017540) postaxial polydactyly of toes, bilateral --> obsolete postaxial polydactyly of toes, bilateral
* [MONDO:0017541](http://purl.obolibrary.org/obo/MONDO_0017541) central polydactyly of toes, unilateral --> obsolete central polydactyly of toes, unilateral
* [MONDO:0017542](http://purl.obolibrary.org/obo/MONDO_0017542) central polydactyly of toes, bilateral --> obsolete central polydactyly of toes, bilateral
* [MONDO:0017678](http://purl.obolibrary.org/obo/MONDO_0017678) disease with punctate palmoplantar keratoderma as a major feature --> obsolete disease with punctate palmoplantar keratoderma as a major feature
* [MONDO:0017679](http://purl.obolibrary.org/obo/MONDO_0017679) autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature --> obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
* [MONDO:0017680](http://purl.obolibrary.org/obo/MONDO_0017680) autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature --> obsolete autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature
* [MONDO:0017820](http://purl.obolibrary.org/obo/MONDO_0017820) disease with Cushing syndrome as a major feature --> obsolete disease with Cushing syndrome as a major feature
* [MONDO:0017938](http://purl.obolibrary.org/obo/MONDO_0017938) X-linked cleft palate and ankyloglossia --> obsolete X-linked cleft palate and ankyloglossia
* [MONDO:0017996](http://purl.obolibrary.org/obo/MONDO_0017996) blepharophimosis - intellectual disability syndrome due to UBE3B deficiency --> obsolete blepharophimosis - intellectual disability syndrome due to UBE3B deficiency
* [MONDO:0018275](http://purl.obolibrary.org/obo/MONDO_0018275) salt and pepper syndrome --> obsolete salt and pepper syndrome
* [MONDO:0018336](http://purl.obolibrary.org/obo/MONDO_0018336) Silver-Russell syndrome due to a point mutation --> obsolete Silver-Russell syndrome due to a point mutation
* [MONDO:0019348](http://purl.obolibrary.org/obo/MONDO_0019348) Ehlers-Danlos syndrome with periventricular heterotopia --> obsolete Ehlers-Danlos syndrome with periventricular heterotopia
* [MONDO:0019389](http://purl.obolibrary.org/obo/MONDO_0019389) X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome --> obsolete X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome
* [MONDO:0019410](http://purl.obolibrary.org/obo/MONDO_0019410) nodulosis-arthropathy-osteolysis syndrome --> obsolete nodulosis-arthropathy-osteolysis syndrome
* [MONDO:0019657](http://purl.obolibrary.org/obo/MONDO_0019657) sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes --> obsolete sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
* [MONDO:0019658](http://purl.obolibrary.org/obo/MONDO_0019658) sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation --> obsolete sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
* [MONDO:0019894](http://purl.obolibrary.org/obo/MONDO_0019894) non-distal monosomy 7p --> obsolete non-distal monosomy 7p
* [MONDO:0020150](http://purl.obolibrary.org/obo/MONDO_0020150) rare palpebral, lacrimal system and conjunctival disease --> obsolete rare palpebral, lacrimal system and conjunctival disease
* [MONDO:0020168](http://purl.obolibrary.org/obo/MONDO_0020168) kinetic eyelid anomaly --> obsolete kinetic eyelid anomaly
* [MONDO:0020170](http://purl.obolibrary.org/obo/MONDO_0020170) congenital upper palpebral retraction --> obsolete congenital upper palpebral retraction
* [MONDO:0020199](http://purl.obolibrary.org/obo/MONDO_0020199) conjunctival vascular anomaly --> obsolete conjunctival vascular anomaly
* [MONDO:0020200](http://purl.obolibrary.org/obo/MONDO_0020200) conjunctival hemangioma or hemolymphangioma --> obsolete conjunctival hemangioma or hemolymphangioma
* [MONDO:0020201](http://purl.obolibrary.org/obo/MONDO_0020201) conjunctival telangiectasia (disease) --> obsolete conjunctival telangiectasia (disease)
* [MONDO:0020202](http://purl.obolibrary.org/obo/MONDO_0020202) conjunctival lymphangiectasia --> obsolete conjunctival lymphangiectasia
* [MONDO:0020261](http://purl.obolibrary.org/obo/MONDO_0020261) neurological disease with abnormal eye movements --> obsolete neurological disease with abnormal eye movements
* [MONDO:0020719](http://purl.obolibrary.org/obo/MONDO_0020719) susceptibility to Hirschsprung disease --> obsolete susceptibility to Hirschsprung disease
* [MONDO:0024236](http://purl.obolibrary.org/obo/MONDO_0024236) degenerative disorder --> obsolete degenerative disorder
* [MONDO:0024624](http://purl.obolibrary.org/obo/MONDO_0024624) atrophy of lacrimal gland --> obsolete atrophy of lacrimal gland
* [MONDO:0033571](http://purl.obolibrary.org/obo/MONDO_0033571) skeletal muscle glycogen content and metabolism quantitative trait locus --> obsolete skeletal muscle glycogen content and metabolism quantitative trait locus
## Renaming
* [MONDO:0000049](http://purl.obolibrary.org/obo/MONDO_0000049) invasive pneumococcal disease, recurrent isolated --> obsolete invasive pneumococcal disease, recurrent isolated
* [MONDO:0000123](http://purl.obolibrary.org/obo/MONDO_0000123) obsolete factor v and Factor VIII, combined deficiency of --> obsolete factor V and Factor VIII, combined deficiency of
* [MONDO:0001807](http://purl.obolibrary.org/obo/MONDO_0001807) familial combined hyperlipidemia --> obsolete familial combined hyperlipidemia
* [MONDO:0001932](http://purl.obolibrary.org/obo/MONDO_0001932) atrophic vulva --> obsolete atrophic vulva
* [MONDO:0002264](http://purl.obolibrary.org/obo/MONDO_0002264) atrophy of prostate --> obsolete atrophy of prostate
* [MONDO:0006168](http://purl.obolibrary.org/obo/MONDO_0006168) common hematopoietic neoplasm --> obsolete common hematopoietic neoplasm
* [MONDO:0006315](http://purl.obolibrary.org/obo/MONDO_0006315) neoplastic medium-sized B-lymphocyte with basophilic cytoplasm --> obsolete neoplastic medium-sized B-lymphocyte with basophilic cytoplasm
* [MONDO:0007347](http://purl.obolibrary.org/obo/MONDO_0007347) CXB3S --> obsolete Coxsackievirus B3 susceptibility
* [MONDO:0007468](http://purl.obolibrary.org/obo/MONDO_0007468) DNA, satellite, alpha type --> obsolete DNA, satellite, alpha type
* [MONDO:0007506](http://purl.obolibrary.org/obo/MONDO_0007506) echo virus 11 sensitivity --> obsoleted echo virus 11 sensitivity
* [MONDO:0008490](http://purl.obolibrary.org/obo/MONDO_0008490) Stickler syndrome type 3 --> otospondylomegaepiphyseal dysplasia, autosomal dominant
* [MONDO:0008535](http://purl.obolibrary.org/obo/MONDO_0008535) telangiectasia, hereditary hemorrhagic, of Rendu, Osler, and Weber --> telangiectasia, hereditary hemorrhagic, type 1
* [MONDO:0008657](http://purl.obolibrary.org/obo/MONDO_0008657) vibratory angioedema --> obsolete vibratory angioedema
* [MONDO:0008659](http://purl.obolibrary.org/obo/MONDO_0008659) transcobalamin i deficiency --> transcobalamin I deficiency
* [MONDO:0008761](http://purl.obolibrary.org/obo/MONDO_0008761) alpha-2-deficient collagen disease --> obsolete alpha-2-deficient collagen disease
* [MONDO:0008885](http://purl.obolibrary.org/obo/MONDO_0008885) Branchioskeletogenital syndrome --> Elsahy-Waters syndrome
* [MONDO:0009304](http://purl.obolibrary.org/obo/MONDO_0009304) Gorlin-Chaudhry-Moss syndrome --> obsolete Gorlin-Chaudhry-Moss syndrome
* [MONDO:0009640](http://purl.obolibrary.org/obo/MONDO_0009640) mitochondrial complex I deficiency, nuclear type --> obsolete mitochondrial complex I deficiency, nuclear type
* [MONDO:0010071](http://purl.obolibrary.org/obo/MONDO_0010071) spondyloenchondrodysplasia --> obsolete spondyloenchondrodysplasia
* [MONDO:0010195](http://purl.obolibrary.org/obo/MONDO_0010195) Weissenbacher-Zweymuller syndrome --> obsolete Weissenbacher-Zweymuller syndrome
* [MONDO:0010272](http://purl.obolibrary.org/obo/MONDO_0010272) syndromic X-linked intellectual disability type 10 --> obsolete syndromic X-linked intellectual disability type 10
* [MONDO:0010327](http://purl.obolibrary.org/obo/MONDO_0010327) HSD10 disease --> HSD10 mitochondrial disease
* [MONDO:0010357](http://purl.obolibrary.org/obo/MONDO_0010357) MRX78 --> obsolete MRX78
* [MONDO:0010376](http://purl.obolibrary.org/obo/MONDO_0010376) Brooks-Wisniewski-brown syndrome --> obsolete Brooks-Wisniewski-brown syndrome
* [MONDO:0010386](http://purl.obolibrary.org/obo/MONDO_0010386) X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency --> immunodeficiency 33
* [MONDO:0010387](http://purl.obolibrary.org/obo/MONDO_0010387) invasive pneumococcal disease, recurrent isolated, 2 --> obsolete invasive pneumococcal disease, recurrent isolated, 2
* [MONDO:0010961](http://purl.obolibrary.org/obo/MONDO_0010961) obesity due to prohormone convertase i deficiency --> obesity due to prohormone convertase I deficiency
* [MONDO:0011324](http://purl.obolibrary.org/obo/MONDO_0011324) hypospadias, hypertelorism, upper 51D coloboma, and mixed-type hearing loss --> obsolete hypospadias, hypertelorism, upper 51D coloboma, and mixed-type hearing loss
* [MONDO:0011859](http://purl.obolibrary.org/obo/MONDO_0011859) distal myopathy with early respiratory muscle involvement --> obsolete distal myopathy with early respiratory muscle involvement
* [MONDO:0012186](http://purl.obolibrary.org/obo/MONDO_0012186) Fanconi anemia complementation group i --> Fanconi anemia complementation group I
* [MONDO:0012189](http://purl.obolibrary.org/obo/MONDO_0012189) Amish infantile epilepsy syndrome --> obsolete Amish infantile epilepsy syndrome
* [MONDO:0012560](http://purl.obolibrary.org/obo/MONDO_0012560) invasive pneumococcal disease, recurrent isolated, 1 --> obsolete invasive pneumococcal disease, recurrent isolated, 1
* [MONDO:0013422](http://purl.obolibrary.org/obo/MONDO_0013422) type i complement component 8 deficiency --> type I complement component 8 deficiency
* [MONDO:0013494](http://purl.obolibrary.org/obo/MONDO_0013494) PSMNSW --> obsolete PSMNSW
* [MONDO:0013701](http://purl.obolibrary.org/obo/MONDO_0013701) MRT32 --> obsolete MRT32
* [MONDO:0014567](http://purl.obolibrary.org/obo/MONDO_0014567) postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome --> glutamate pyruvate transaminase 2 deficiency
* [MONDO:0014985](http://purl.obolibrary.org/obo/MONDO_0014985) Fanconi anemia complementation group v --> Fanconi anemia complementation group V
* [MONDO:0015172](http://purl.obolibrary.org/obo/MONDO_0015172) epithelio-exfoliative colitis-deafness syndrome --> obsolete epithelio-exfoliative colitis-deafness syndrome
* [MONDO:0015173](http://purl.obolibrary.org/obo/MONDO_0015173) autoimmune enteropathy type 2 --> obsolete autoimmune enteropathy type 2
* [MONDO:0015297](http://purl.obolibrary.org/obo/MONDO_0015297) microcephaly-digital anomalies-intellectual disability syndrome --> obsolete microcephaly-digital anomalies-intellectual disability syndrome
* [MONDO:0015560](http://purl.obolibrary.org/obo/MONDO_0015560) classic mast cell leukemia --> obsolete classic mast cell leukemia
* [MONDO:0015602](http://purl.obolibrary.org/obo/MONDO_0015602) developmental delay-deafness syndrome, Hildebrand type --> obsolete developmental delay-deafness syndrome, Hildebrand type
* [MONDO:0015964](http://purl.obolibrary.org/obo/MONDO_0015964) rare genetic palpebral, lacrimal system and conjunctival disease --> obsolete rare genetic palpebral, lacrimal system and conjunctival disease
* [MONDO:0016082](http://purl.obolibrary.org/obo/MONDO_0016082) tracheo-esophageal fistula-hypospadias syndrome --> obsolete tracheo-esophageal fistula-hypospadias syndrome
* [MONDO:0016111](http://purl.obolibrary.org/obo/MONDO_0016111) non-dystrophic myopathy with collagen 6 anomaly --> obsolete non-dystrophic myopathy with collagen 6 anomaly
* [MONDO:0016124](http://purl.obolibrary.org/obo/MONDO_0016124) drug and/or toxic myopathy --> obsolete drug and/or toxic myopathy
* [MONDO:0016997](http://purl.obolibrary.org/obo/MONDO_0016997) hereditary epidermolysis bullosa associated with ocular features --> obsolete hereditary epidermolysis bullosa associated with ocular features
* [MONDO:0017378](http://purl.obolibrary.org/obo/MONDO_0017378) polymicrogyria-turricephaly-hypogenitalism syndrome --> obsolete polymicrogyria-turricephaly-hypogenitalism syndrome
* [MONDO:0017458](http://purl.obolibrary.org/obo/MONDO_0017458) postaxial polydactyly of toes --> obsolete postaxial polydactyly of toes
* [MONDO:0017459](http://purl.obolibrary.org/obo/MONDO_0017459) central polydactyly of toes --> obsolete central polydactyly of toes
* [MONDO:0017494](http://purl.obolibrary.org/obo/MONDO_0017494) congenital absence of upper arm and forearm with hand present, unilateral --> obsolete congenital absence of upper arm and forearm with hand present, unilateral
* [MONDO:0017495](http://purl.obolibrary.org/obo/MONDO_0017495) congenital absence of upper arm and forearm with hand present, bilateral --> obsolete congenital absence of upper arm and forearm with hand present, bilateral
* [MONDO:0017539](http://purl.obolibrary.org/obo/MONDO_0017539) postaxial polydactyly of toes, unilateral --> obsolete postaxial polydactyly of toes, unilateral
* [MONDO:0017540](http://purl.obolibrary.org/obo/MONDO_0017540) postaxial polydactyly of toes, bilateral --> obsolete postaxial polydactyly of toes, bilateral
* [MONDO:0017541](http://purl.obolibrary.org/obo/MONDO_0017541) central polydactyly of toes, unilateral --> obsolete central polydactyly of toes, unilateral
* [MONDO:0017542](http://purl.obolibrary.org/obo/MONDO_0017542) central polydactyly of toes, bilateral --> obsolete central polydactyly of toes, bilateral
* [MONDO:0017678](http://purl.obolibrary.org/obo/MONDO_0017678) disease with punctate palmoplantar keratoderma as a major feature --> obsolete disease with punctate palmoplantar keratoderma as a major feature
* [MONDO:0017679](http://purl.obolibrary.org/obo/MONDO_0017679) autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature --> obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
* [MONDO:0017680](http://purl.obolibrary.org/obo/MONDO_0017680) autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature --> obsolete autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature
* [MONDO:0017820](http://purl.obolibrary.org/obo/MONDO_0017820) disease with Cushing syndrome as a major feature --> obsolete disease with Cushing syndrome as a major feature
* [MONDO:0017938](http://purl.obolibrary.org/obo/MONDO_0017938) X-linked cleft palate and ankyloglossia --> obsolete X-linked cleft palate and ankyloglossia
* [MONDO:0017996](http://purl.obolibrary.org/obo/MONDO_0017996) blepharophimosis - intellectual disability syndrome due to UBE3B deficiency --> obsolete blepharophimosis - intellectual disability syndrome due to UBE3B deficiency
* [MONDO:0018275](http://purl.obolibrary.org/obo/MONDO_0018275) salt and pepper syndrome --> obsolete salt and pepper syndrome
* [MONDO:0018336](http://purl.obolibrary.org/obo/MONDO_0018336) Silver-Russell syndrome due to a point mutation --> obsolete Silver-Russell syndrome due to a point mutation
* [MONDO:0019348](http://purl.obolibrary.org/obo/MONDO_0019348) Ehlers-Danlos syndrome with periventricular heterotopia --> obsolete Ehlers-Danlos syndrome with periventricular heterotopia
* [MONDO:0019389](http://purl.obolibrary.org/obo/MONDO_0019389) X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome --> obsolete X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome
* [MONDO:0019410](http://purl.obolibrary.org/obo/MONDO_0019410) nodulosis-arthropathy-osteolysis syndrome --> obsolete nodulosis-arthropathy-osteolysis syndrome
* [MONDO:0019657](http://purl.obolibrary.org/obo/MONDO_0019657) sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes --> obsolete sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
* [MONDO:0019658](http://purl.obolibrary.org/obo/MONDO_0019658) sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation --> obsolete sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
* [MONDO:0019894](http://purl.obolibrary.org/obo/MONDO_0019894) non-distal monosomy 7p --> obsolete non-distal monosomy 7p
* [MONDO:0020150](http://purl.obolibrary.org/obo/MONDO_0020150) rare palpebral, lacrimal system and conjunctival disease --> obsolete rare palpebral, lacrimal system and conjunctival disease
* [MONDO:0020168](http://purl.obolibrary.org/obo/MONDO_0020168) kinetic eyelid anomaly --> obsolete kinetic eyelid anomaly
* [MONDO:0020170](http://purl.obolibrary.org/obo/MONDO_0020170) congenital upper palpebral retraction --> obsolete congenital upper palpebral retraction
* [MONDO:0020199](http://purl.obolibrary.org/obo/MONDO_0020199) conjunctival vascular anomaly --> obsolete conjunctival vascular anomaly
* [MONDO:0020200](http://purl.obolibrary.org/obo/MONDO_0020200) conjunctival hemangioma or hemolymphangioma --> obsolete conjunctival hemangioma or hemolymphangioma
* [MONDO:0020201](http://purl.obolibrary.org/obo/MONDO_0020201) conjunctival telangiectasia (disease) --> obsolete conjunctival telangiectasia (disease)
* [MONDO:0020202](http://purl.obolibrary.org/obo/MONDO_0020202) conjunctival lymphangiectasia --> obsolete conjunctival lymphangiectasia
* [MONDO:0020261](http://purl.obolibrary.org/obo/MONDO_0020261) neurological disease with abnormal eye movements --> obsolete neurological disease with abnormal eye movements
* [MONDO:0020719](http://purl.obolibrary.org/obo/MONDO_0020719) susceptibility to Hirschsprung disease --> obsolete susceptibility to Hirschsprung disease
* [MONDO:0022932](http://purl.obolibrary.org/obo/MONDO_0022932) davenport-Donlan syndrome --> Davenport-Donlan syndrome
* [MONDO:0024236](http://purl.obolibrary.org/obo/MONDO_0024236) degenerative disorder --> obsolete degenerative disorder
* [MONDO:0024624](http://purl.obolibrary.org/obo/MONDO_0024624) atrophy of lacrimal gland --> obsolete atrophy of lacrimal gland
* [MONDO:0033571](http://purl.obolibrary.org/obo/MONDO_0033571) skeletal muscle glycogen content and metabolism quantitative trait locus --> obsolete skeletal muscle glycogen content and metabolism quantitative trait locus