Experimental Factor Ontology
6778 terms(s) returned
| Term Type: | Record: 6651 to 6700 of 6778 Records | Page: 134 of 136, First Previous Next Last | Show Records Per Page |
- 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 lymphoproliferative disease
- 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 nemaline myopathy
- autosomal recessive non-syndromic intellectual disability
- autosomal recessive nonsyndromic hearing loss 102
- autosomal recessive nonsyndromic hearing loss 124
- autosomal recessive nonsyndromic hearing loss 18A
- autosomal recessive nonsyndromic hearing loss 1A
- autosomal recessive nonsyndromic hearing loss 1B
- autosomal recessive nonsyndromic hearing loss 2
- autosomal recessive nonsyndromic hearing loss 23
- autosomal recessive nonsyndromic hearing loss 30
- autosomal recessive nonsyndromic hearing loss 31
- autosomal recessive nonsyndromic hearing loss 4
- autosomal recessive nonsyndromic hearing loss 53
- autosomal recessive nonsyndromic hearing loss 63
- autosomal recessive nonsyndromic hearing loss 7
- autosomal recessive nonsyndromic hearing loss 70
- autosomal recessive nonsyndromic hearing loss 86
- autosomal recessive nonsyndromic hearing loss 89
- autosomal recessive nonsyndromic hearing loss 9
- autosomal recessive nonsyndromic hearing loss 97
- autosomal recessive nonsyndromic hearing loss 98
- autosomal recessive ocular albinism
- autosomal recessive omodysplasia
- autosomal recessive optic atrophy
- autosomal recessive optic atrophy, OPA7 type
- autosomal recessive osteopetrosis
- autosomal recessive osteopetrosis 1
- autosomal recessive osteopetrosis 2
- autosomal recessive osteopetrosis 3
- autosomal recessive osteopetrosis 4
- autosomal recessive osteopetrosis 6
- autosomal recessive osteopetrosis 7
- autosomal recessive palmoplantar keratoderma and congenital alopecia
- autosomal recessive polycystic kidney disease
- autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
- autosomal recessive primary microcephaly
- autosomal recessive progressive external ophthalmoplegia
- autosomal recessive proximal renal tubular acidosis
- autosomal recessive retinitis pigmentosa
- autosomal recessive secondary polycythemia not associated with VHL gene
