Mondo Disease Ontology
5946 terms(s) returned
| Term Type: | Record: 5801 to 5850 of 5946 Records | Page: 117 of 119, First Previous Next Last | Show Records Per Page |
- autosomal recessive nonsyndromic hearing loss 66
- autosomal recessive nonsyndromic hearing loss 67
- autosomal recessive nonsyndromic hearing loss 68
- autosomal recessive nonsyndromic hearing loss 7
- autosomal recessive nonsyndromic hearing loss 70
- autosomal recessive nonsyndromic hearing loss 71
- autosomal recessive nonsyndromic hearing loss 74
- autosomal recessive nonsyndromic hearing loss 76
- autosomal recessive nonsyndromic hearing loss 77
- autosomal recessive nonsyndromic hearing loss 79
- autosomal recessive nonsyndromic hearing loss 8
- autosomal recessive nonsyndromic hearing loss 83
- autosomal recessive nonsyndromic hearing loss 84A
- autosomal recessive nonsyndromic hearing loss 84B
- autosomal recessive nonsyndromic hearing loss 85
- autosomal recessive nonsyndromic hearing loss 86
- autosomal recessive nonsyndromic hearing loss 88
- autosomal recessive nonsyndromic hearing loss 89
- autosomal recessive nonsyndromic hearing loss 9
- autosomal recessive nonsyndromic hearing loss 91
- autosomal recessive nonsyndromic hearing loss 93
- autosomal recessive nonsyndromic hearing loss 96
- autosomal recessive nonsyndromic hearing loss 97
- autosomal recessive nonsyndromic hearing loss 98
- autosomal recessive ocular albinism
- autosomal recessive omodysplasia
- 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 5
- autosomal recessive osteopetrosis 6
- autosomal recessive osteopetrosis 7
- autosomal recessive osteopetrosis 8
- autosomal recessive palmoplantar keratoderma and congenital alopecia
- autosomal recessive pericentral pigmentary retinopathy
- 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 secondary polycythemia not associated with VHL gene
- autosomal recessive severe congenital neutropenia
- autosomal recessive severe congenital neutropenia due to CSF3R deficiency
- autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
- autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
- autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
- autosomal recessive sideroblastic anemia
