Human Disease Ontology
19719 terms(s) returned
| Term Type: | Record: 3401 to 3450 of 19719 Records | Page: 69 of 395, First Previous Next Last | Show Records Per Page |
- Wolffian duct adenoma
- Wolfram syndrome
- Wolfram syndrome 1
- Wolfram syndrome 2
- Wolfram syndrome, mitochondrial form
- Wolman disease
- Woodhouse-Sakati syndrome
- Worth syndrome
- X-Linked immunodeficiency 74
- X-linked Aarskog syndrome
- X-linked Alport syndrome
- X-linked Emery-Dreifuss muscular dystrophy 1
- X-linked Emery-Dreifuss muscular dystrophy 6
- X-linked VACTERL association
- X-linked adrenal hypoplasia congenita
- X-linked agammaglobulinemia
- X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
- X-linked atrophic macular degeneration
- X-linked cardiac valvular dysplasia
- X-linked central diabetes insipidus
- X-linked cerebellar ataxia
- X-linked chondrodysplasia punctata 1
- X-linked chondrodysplasia punctata 2
- X-linked chronic granulomatous disease
- X-linked chronic idiopathic intestinal pseudo-obstruction
- X-linked cleft palate with or without ankyloglossia
- X-linked cone-rod dystrophy 1
- X-linked cone-rod dystrophy 2
- X-linked cone-rod dystrophy 3
- X-linked congenital bilateral absence of vas deferens
- X-linked congenital hemolytic anemia
- X-linked congenital hydrocephalus
- X-linked congenital myopathy with fiber-type disproportion
- X-linked deafness 1
- X-linked deafness 2
- X-linked deafness 3
- X-linked deafness 4
- X-linked deafness 5
- X-linked deafness 6
- X-linked deafness 7
- X-linked distal spinal muscular atrophy 3
- X-linked dominant disease
- X-linked dominant inheritance
- X-linked dyserythropoietic anemia
- X-linked dyskeratosis congenita
- X-linked dystonia-parkinsonism
- X-linked endothelial corneal dystrophy
- X-linked epilepsy with variable learning disabilities and behavior disorders
- X-linked exudative vitreoretinopathy 2
- X-linked hereditary ataxia
