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Summary Literature (1)
MIM:610474 - CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME; CATSHLS

Xenbase Genes: fgfr3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012504 - camptodactyly-tall stature-scoliosis-hearing loss syndrome

Disease Ontology (DO):
DOID:0111160 - camptodactyly-tall stature-scoliosis-hearing loss syndrome