Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 3951 to 4000 of 11113 Records | Page: 80 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_autosomal recessive distal renal tubular acidosis
- obsolete_autosomal recessive frontotemporal pachygyria
- obsolete_autosomal recessive hereditary demyelinating motor and sensory neuropathy
- obsolete_autosomal recessive hereditary sensory and autonomic neuropathy
- obsolete_autosomal recessive hyperinsulinism due to Kir6.2 deficiency
- obsolete_autosomal recessive hyperinsulinism due to SUR1 deficiency
- obsolete_autosomal recessive hypohidrotic ectodermal dysplasia
- obsolete_autosomal recessive hypophosphatemic rickets
- obsolete_autosomal recessive intermediate Charcot-Marie-Tooth disease
- obsolete_autosomal recessive isolated diffuse palmoplantar keratoderma
- obsolete_autosomal recessive limb-girdle muscular dystrophy
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2A
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2B
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2C
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2D
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2E
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2F
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2G
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2H
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2I
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2J
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2K
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2L
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2M
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2N
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2O
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2P
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2Q
- obsolete_autosomal recessive limb-girdle muscular dystrophy type 2T
- obsolete_autosomal recessive lower motor neuron disease with childhood onset
- obsolete_autosomal recessive lymphoproliferative disease
- obsolete_autosomal recessive metabolic cerebellar ataxia
- obsolete_autosomal recessive multiple pterygium syndrome
- obsolete_autosomal recessive myogenic arthrogryposis multiplex congenita
- obsolete_autosomal recessive non-syndromic intellectual disability
- obsolete_autosomal recessive omodysplasia
- obsolete_autosomal recessive optic atrophy
- obsolete_autosomal recessive optic atrophy, OPA7 type
- obsolete_autosomal recessive palmoplantar keratoderma and congenital alopecia
- obsolete_autosomal recessive polycystic kidney disease
- obsolete_autosomal recessive primary microcephaly
- obsolete_autosomal recessive progressive external ophthalmoplegia
- obsolete_autosomal recessive proximal renal tubular acidosis
- obsolete_autosomal recessive pure spastic paraplegia
- obsolete_autosomal recessive secondary polycythemia not associated with VHL gene
- obsolete_autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
- obsolete_autosomal recessive sideroblastic anemia
- obsolete_autosomal recessive spastic ataxia
- obsolete_autosomal recessive spastic paraplegia type 59
- obsolete_autosomal recessive spastic paraplegia type 60
