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.

Also known as: 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

36 clinical trials for this condition and its sub-types.

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