Disease #00595 (Hypochondroplasia, OMIM:146000)

Official abbreviation -
Name Hypochondroplasia
OMIM ID 146000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene FGFR3
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00306132 66 - - M - China - - - - - Hypochondroplasia - FGFR3 FGFR3 1 1 Sha Hong
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