Disease #00594 (ACH (achondroplasia (ACH)), OMIM:100800)

Official abbreviation ACH
Name achondroplasia (ACH)
OMIM ID 100800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FGFR3
Associated tissues -
Disease features -
Remarks -