Experimental Factor Ontology
3875 terms(s) returned
| Term Type: | Record: 3701 to 3750 of 3875 Records | Page: 75 of 78, First Previous Next Last | Show Records Per Page |
- autosomal recessive brachyolmia
- autosomal recessive centronuclear myopathy
- autosomal recessive cerebellar ataxia
- autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
- autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome
- autosomal recessive cerebellar ataxia with late-onset spasticity
- autosomal recessive cerebellar ataxia-blindness-deafness syndrome
- autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
- autosomal recessive cerebral atrophy
- autosomal recessive complex spastic paraplegia
- autosomal recessive complex spastic paraplegia type 9B
- autosomal recessive cone rod dystrophy
- autosomal recessive congenital cerebellar ataxia
- autosomal recessive congenital ichthyosis
- autosomal recessive congenital ichthyosis 11
- autosomal recessive congenital ichthyosis 4A
- autosomal recessive congenital ichthyosis 4B
- autosomal recessive congenital stationary night blindness
- 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 degenerative and progressive cerebellar ataxia
- autosomal recessive dilated cardiomyopathy
- 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 dyskeratosis congenita 4
- autosomal recessive epidermolytic ichthyosis
- autosomal recessive faciodigitogenital syndrome
- autosomal recessive familial Mediterranean fever
- autosomal recessive frontotemporal pachygyria
- autosomal recessive hereditary demyelinating motor and sensory neuropathy
- autosomal recessive hereditary sensory and autonomic neuropathy
- autosomal recessive humeroradial synostosis
- 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 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
