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Hypophosphatemic Rickets, Autosomal Recessive, 2 (MONDO:0013219)

Any autosomal recessive hypophosphatemic rickets in which the cause of the disease is a mutation in the ENPP1 gene.

Overview

Category

Ontology ID

Internal:14255

Synonyms

Autosomal Recessive Hypophosphatemic Rickets Type 2

ENPP1 autosomal recessive hypophosphatemic rickets

autosomal recessive hypophosphatemic rickets caused by mutation in ENPP1

hypophosphatemic rickets, autosomal recessive, 2

hypophosphatemic rickets, autosomal recessive, type 2

ARHR2

Mapped terms

GARD:0018417

MEDGEN:442380

MESH:C567647

NORD:2000

OMIM:613312

UMLS:C2750078

Child terms

Unknown children.