Hypophosphatemic rickets, autosomal recessive, 2

rare

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

Identifiers: MONDO:0013219 OMIM:613312
Causal genes: ENPP1
Part of: Abnormal mineralization disorder Autosomal recessive hypophosphatemic rickets
Also known as: ARHR2 · autosomal recessive hypophosphatemic rickets caused by mutation in ENPP1 · Autosomal Recessive Hypophosphatemic Rickets Type 2 · ENPP1 autosomal recessive hypophosphatemic rickets · hypophosphatemic rickets, autosomal recessive, type 2

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