Experimental Factor Ontology
136 terms(s) returned
Term Type: Class | Record: 101 to 136 of 136 Records | Page: 3 of 3, First Previous Next Last | Show Records Per Page |
- X-linked recessive disease
- X-linked recessive mitochondrial myopathy
- X-linked recessive ocular albinism
- X-linked reticulate pigmentary disorder
- X-linked retinal dysplasia
- X-linked retinoschisis
- X-linked severe congenital neutropenia
- X-linked sideroblastic anemia 1
- X-linked sideroblastic anemia with ataxia
- X-linked spasticity-intellectual disability-epilepsy syndrome
- X-linked spinocerebellar ataxia type 3
- X-linked spinocerebellar ataxia type 4
- X-linked spondyloepimetaphyseal dysplasia
- X-linked syndromic intellectual disability
- XFE progeroid syndrome
- XY type gonadal dysgenesis-associated anomalies syndrome
- XYLT1-congenital disorder of glycosylation
- Xp22.13p22.2 duplication syndrome
- Xp22.3 microdeletion syndrome
- Xq12-q13.3 duplication syndrome
- Xq25 microduplication syndrome
- Xq27.3q28 duplication syndrome
- xanthinuria
- xanthinuria type I
- xanthinuria type II
- xanthomatosis
- xeroderma pigmentosum
- xeroderma pigmentosum group A
- xeroderma pigmentosum group B
- xeroderma pigmentosum group C
- xeroderma pigmentosum group D
- xeroderma pigmentosum group E
- xeroderma pigmentosum group F
- xeroderma pigmentosum group G
- xeroderma pigmentosum variant type
- xeroderma pigmentosum-Cockayne syndrome complex