Mondo Disease Ontology
5924 terms(s) returned
| Term Type: | Record: 5651 to 5700 of 5924 Records | Page: 114 of 119, First Previous Next Last | Show Records Per Page |
- autosomal recessive congenital ichthyosis 3
- autosomal recessive congenital ichthyosis 4A
- autosomal recessive congenital ichthyosis 4B
- autosomal recessive congenital ichthyosis 5
- autosomal recessive congenital ichthyosis 6
- autosomal recessive congenital ichthyosis 7
- autosomal recessive congenital ichthyosis 8
- autosomal recessive congenital ichthyosis 9
- autosomal recessive cutis laxa type 1
- autosomal recessive cutis laxa type 2
- autosomal recessive cutis laxa type 2, classic type
- autosomal recessive cutis laxa type 2A
- autosomal recessive cutis laxa type 2B
- autosomal recessive cutis laxa type 2C
- autosomal recessive cutis laxa type 2D
- autosomal recessive cystinuria, SLC3A1-related, dog
- autosomal recessive degenerative and progressive cerebellar ataxia
- autosomal recessive disease
- autosomal recessive distal osteolysis syndrome
- autosomal recessive distal renal tubular acidosis
- autosomal recessive distal spinal muscular atrophy 1
- autosomal recessive distal spinal muscular atrophy 2
- autosomal recessive distal titinopathy
- autosomal recessive dyskeratosis congenita 4
- autosomal recessive early-onset Parkinson disease 23
- autosomal recessive early-onset Parkinson disease 6
- autosomal recessive early-onset Parkinson disease 7
- autosomal recessive epidermolytic ichthyosis
- autosomal recessive extra-oral halitosis
- 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
