hypochondroplasia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
hypochondroplasia
FGFR3 Causal
10215410 11015576 11055896 16912704 7670477 8589686 9452043
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with hypochondroplasia.
5 View disease cluster →
Achondroplasia 1 shared geneFGFR3 Related via 1 shared gene including FGFR3. Camptodactyly, tall stature, and hearing loss syndrome 1 shared geneFGFR3 Related via 1 shared gene including FGFR3. Catshl syndrome 1 shared geneFGFR3 Related via 1 shared gene including FGFR3. Crouzon syndrome with acanthosis nigricans 1 shared geneFGFR3 Related via 1 shared gene including FGFR3. Muenke syndrome 1 shared geneFGFR3 Related via 1 shared gene including FGFR3.