Disease #00035 (HCH (HYPOCHONDROPLASIA), OMIM:146000)

Official abbreviation HCH
Name HYPOCHONDROPLASIA
OMIM ID 146000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FGFR3
Associated tissues -
Disease features -
Remarks -
Date created 2016-07-11 10:34:58 +00:00 (UTC)
Date last edited N/A

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