Experimental Factor Ontology
771 terms(s) returned
| Term Type: | Record: 501 to 550 of 771 Records | Page: 11 of 16, First Previous Next Last | Show Records Per Page |
- X-box-binding protein 1
- X-linked Alport syndrome
- X-linked Charcot-Marie-Tooth disease
- X-linked Charcot-Marie-Tooth disease type 1
- X-linked Charcot-Marie-Tooth disease type 2
- X-linked Charcot-Marie-Tooth disease type 3
- X-linked Charcot-Marie-Tooth disease type 4
- X-linked Charcot-Marie-Tooth disease type 5
- X-linked Charcot-Marie-Tooth disease type 6
- X-linked Ehlers-Danlos syndrome
- X-linked Emery-Dreifuss muscular dystrophy
- X-linked Mendelian susceptibility to mycobacterial diseases
- X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
- X-linked Opitz G/BBB syndrome
- X-linked acrogigantism due to Xq26 microduplication
- X-linked adrenal hypoplasia congenita
- X-linked adrenoleukodystrophy
- X-linked agammaglobulinemia
- X-linked calvarial hyperostosis
- X-linked central congenital hypothyroidism with late-onset testicular enlargement
- X-linked cerebellar ataxia
- X-linked cerebral adrenoleukodystrophy
- X-linked cerebral-cerebellar-coloboma syndrome syndrome
- X-linked chondrodysplasia punctata
- X-linked chondrodysplasia punctata 1
- X-linked chondrodysplasia punctata 2
- X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome
- X-linked complex neurodevelopmental disorder
- X-linked complicated corpus callosum dysgenesis
- X-linked complicated spastic paraplegia type 1
- X-linked cone dysfunction syndrome with myopia
- X-linked cone-rod dystrophy
- X-linked cone-rod dystrophy 1
- X-linked cone-rod dystrophy 3
- X-linked congenital disorder of glycosylation with intellectual disability as a major feature
- X-linked congenital generalized hypertrichosis
- X-linked congenital stationary night blindness
- X-linked corneal dermoid
- X-linked creatine transporter deficiency
- X-linked deafness
- X-linked diffuse leiomyomatosis - Alport syndrome
- X-linked diffuse leiomyomatosis-Alport syndrome
- X-linked disease
- X-linked distal arthrogryposis multiplex congenita
- X-linked distal hereditary motor neuropathy
- X-linked distal spinal muscular atrophy type 3
- X-linked dominant chondrodysplasia punctata
- X-linked dominant chondrodysplasia, Chassaing-Lacombe type
- X-linked dominant disease
- X-linked dominant hypophosphatemic rickets
