OBO ID: DOID:0080353
Term Name: X-linked recessive hypophosphatemic rickets Search Ontology:
Synonyms:
Definition: A rickets that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11.22. https://ghr.nlm.nih.gov/condition/hereditary-hypophosphatemic-rickets
References:
Ontology: Human Disease   ( DOID:0080353 )
OTHER X-linked recessive hypophosphatemic rickets PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLCN5 Hypophosphatemic rickets 300554
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None