Disease #00250 (hypophosphatemic rickets, X-linked recessive (HPXR), OMIM:300554)

Official abbreviation -
Name hypophosphatemic rickets, X-linked recessive (HPXR)
OMIM ID 300554
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CLCN5
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Disease features -
Remarks -
Date created 2013-10-20 13:24:02 +02:00 (CEST)
Date last edited N/A