Human Disease Ontology
2240 terms(s) returned
| Term Type: | Record: 1851 to 1900 of 2240 Records | Page: 38 of 45, First Previous Next Last | Show Records Per Page |
- 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
- autosomal dominant tubulointerstitial kidney disease 1
- autosomal dominant tubulointerstitial kidney disease 2
- autosomal dominant tubulointerstitial kidney disease 4
- autosomal dominant tubulointerstitial kidney disease 5
- autosomal dominant tubulointerstitial kidney disease 6
- autosomal dominant vitreoretinochoroidopathy
- autosomal dominant woolly hair
- autosomal genetic disease
- autosomal hemophilia A
- autosomal inheritance
- autosomal recessive Emery-Dreifuss muscular dystrophy 3
- autosomal recessive Robinow syndrome
- autosomal recessive Robinow syndrome 2
- autosomal recessive Segawa syndrome
- autosomal recessive Whistling face syndrome
- autosomal recessive autoinflammation, panniculitis, and dermatosis syndrome
- autosomal recessive axonal Charcot-Marie-Tooth disease with vocal cord paresis
- autosomal recessive brain small vessel disease 2B
- autosomal recessive centronuclear myopathy
- autosomal recessive cerebellar ataxia
- autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1
- autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 2
- autosomal recessive chronic granulomatous disease 1
- autosomal recessive chronic granulomatous disease 2
- autosomal recessive chronic granulomatous disease 3
