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X-Linked Dominant Hypophosphatemic Rickets (MONDO:0010619)

X-linked hypophosphatemia (XLH) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia, and diminished growth.

Overview

Category

musculoskeletal system disorder

Ontology ID

MONDO:0010619

Internal:11766

Synonyms

X-linked hypophosphatemia

X-linked hypophosphatemic rickets

X-linked dominant hypophosphatemic rickets

X-linked hereditary hypophosphatemic rickets

XLH

hereditary hypophosphatemic rickets, X-linked

hypophosphatemic rickets, X-linked

hypophosphatemic rickets, X-linked dominant, X-linked dominant

rickets, vitamin D-resistant

vitamin D-resistant rickets, X-linked

HPDR

HYP

XLHR

hypophophatemia, X-linked

hypophophatemic vitamin D-resistant rickets

hypophosphatemia, X-linked

hypophosphatemic rickets, X-linked dominant

hypophosphatemic vitamin D-resistant rickets

Mapped terms

DOID:0050445

GARD:0012943

MEDGEN:196551

NANDO:1200779

NCIT:C85234

OMIM:307800

Orphanet:89936

SCTID:82236004

UMLS:C0733682

Child terms

Unknown children.

Results

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