Mondo Disease Ontology
5946 terms(s) returned
| Term Type: | Record: 5701 to 5750 of 5946 Records | Page: 115 of 119, First Previous Next Last | Show Records Per Page |
- autosomal recessive faciodigitogenital syndrome
- autosomal recessive familial Mediterranean fever
- autosomal recessive frontotemporal pachygyria
- autosomal recessive humeroradial synostosis
- autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius
- autosomal recessive hyperinsulinism due to Kir6.2 deficiency
- autosomal recessive hyperinsulinism due to SUR1 deficiency
- autosomal recessive hypohidrotic ectodermal dysplasia
- autosomal recessive hypophosphatemic rickets
- autosomal recessive inherited pseudoxanthoma elasticum
- autosomal recessive intermediate Charcot-Marie-Tooth disease
- autosomal recessive juvenile Parkinson disease 2
- autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome
- autosomal recessive limb-girdle muscular dystrophy
- autosomal recessive limb-girdle muscular dystrophy type 2A
- autosomal recessive limb-girdle muscular dystrophy type 2B
- autosomal recessive limb-girdle muscular dystrophy type 2C
- autosomal recessive limb-girdle muscular dystrophy type 2D
- autosomal recessive limb-girdle muscular dystrophy type 2E
- autosomal recessive limb-girdle muscular dystrophy type 2F
- autosomal recessive limb-girdle muscular dystrophy type 2G
- autosomal recessive limb-girdle muscular dystrophy type 2H
- autosomal recessive limb-girdle muscular dystrophy type 2I
- autosomal recessive limb-girdle muscular dystrophy type 2J
- autosomal recessive limb-girdle muscular dystrophy type 2K
- autosomal recessive limb-girdle muscular dystrophy type 2L
- autosomal recessive limb-girdle muscular dystrophy type 2M
- autosomal recessive limb-girdle muscular dystrophy type 2N
- autosomal recessive limb-girdle muscular dystrophy type 2O
- autosomal recessive limb-girdle muscular dystrophy type 2P
- autosomal recessive limb-girdle muscular dystrophy type 2Q
- autosomal recessive limb-girdle muscular dystrophy type 2R1
- autosomal recessive limb-girdle muscular dystrophy type 2T
- autosomal recessive limb-girdle muscular dystrophy type 2U
- autosomal recessive limb-girdle muscular dystrophy type 2W
- autosomal recessive limb-girdle muscular dystrophy type 2X
- autosomal recessive limb-girdle muscular dystrophy type 2Y
- autosomal recessive limb-girdle muscular dystrophy type R18
- autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
- autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiency
- autosomal recessive metabolic cerebellar ataxia
- autosomal recessive multiple pterygium syndrome
- autosomal recessive myogenic arthrogryposis multiplex congenita
- autosomal recessive non-syndromic intellectual disability
- autosomal recessive nonsyndromic congenital nuclear cataract
- autosomal recessive nonsyndromic hearing loss 101
- autosomal recessive nonsyndromic hearing loss 102
- autosomal recessive nonsyndromic hearing loss 103
- autosomal recessive nonsyndromic hearing loss 104
- autosomal recessive nonsyndromic hearing loss 12
