Disease #00022 (ISS (SHORT STATURE, IDIOPATHIC, X-LINKED), OMIM:300582)

Official abbreviation ISS
Name SHORT STATURE, IDIOPATHIC, X-LINKED
OMIM ID 300582
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SHOX
Associated tissues -
Disease features -
Remarks -
Date created 2016-07-08 14:51:49 +00:00 (UTC)
Date last edited N/A

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