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Hypophosphatemic Rickets, X-Linked Recessive (MONDO:0010358)

Any X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene.

Overview

Category

Ontology ID

Internal:11524

Synonyms

CLCN5 X-linked hypophosphatemic rickets

X-linked hypophosphatemic rickets caused by mutation in CLCN5

hypophosphatemic rickets, X-linked recessive

Mapped terms

DOID:0080353

GARD:0015011

MEDGEN:335115

OMIM:300554

UMLS:C1845168

Child terms

Unknown children.