Disease #00597 (Crouzon syndrome, with acanthosis nigricans, OMIM:612247)

Official abbreviation -
Name Crouzon syndrome, with acanthosis nigricans
OMIM ID 612247
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FGFR3
Associated tissues -
Disease features -
Remarks -

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