Human Disease Ontology
2205 terms(s) returned
| Term Type: | Record: 1801 to 1850 of 2205 Records | Page: 37 of 45, First Previous Next Last | Show Records Per Page |
- autosomal dominant nonsyndromic deafness 6
- autosomal dominant nonsyndromic deafness 64
- autosomal dominant nonsyndromic deafness 65
- autosomal dominant nonsyndromic deafness 66
- autosomal dominant nonsyndromic deafness 67
- autosomal dominant nonsyndromic deafness 68
- autosomal dominant nonsyndromic deafness 69
- autosomal dominant nonsyndromic deafness 7
- autosomal dominant nonsyndromic deafness 70
- autosomal dominant nonsyndromic deafness 71
- autosomal dominant nonsyndromic deafness 72
- autosomal dominant nonsyndromic deafness 73
- autosomal dominant nonsyndromic deafness 74
- autosomal dominant nonsyndromic deafness 75
- autosomal dominant nonsyndromic deafness 76
- autosomal dominant nonsyndromic deafness 77
- autosomal dominant nonsyndromic deafness 78
- autosomal dominant nonsyndromic deafness 79
- autosomal dominant nonsyndromic deafness 80
- autosomal dominant nonsyndromic deafness 81
- autosomal dominant nonsyndromic deafness 82
- autosomal dominant nonsyndromic deafness 83
- autosomal dominant nonsyndromic deafness 84
- autosomal dominant nonsyndromic deafness 85
- autosomal dominant nonsyndromic deafness 86
- autosomal dominant nonsyndromic deafness 87
- autosomal dominant nonsyndromic deafness 88
- autosomal dominant nonsyndromic deafness 89
- autosomal dominant nonsyndromic deafness 9
- autosomal dominant nonsyndromic deafness 90
- autosomal dominant osteopetrosis 1
- autosomal dominant osteopetrosis 2
- autosomal dominant polycystic kidney disease
- autosomal dominant primary microcephaly
- autosomal dominant primary microcephaly 26
- autosomal dominant primary microcephaly 27
- autosomal dominant progressive external ophthalmoplegia 1
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6
- autosomal dominant pseudohypoaldosteronism type 1
- autosomal dominant sensory ataxia 1
- autosomal dominant severe congenital neutropenia
- autosomal dominant sideroblastic anemia 4
- autosomal dominant spondyloepiphyseal dysplasia tarda
- autosomal dominant thrombophilia due to protein C deficiency
- autosomal dominant thrombophilia due to protein S deficiency
- autosomal dominant tubulointerstitial kidney disease
