Acrocephalosyndactyly type v

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Subtype of: Acrocephalopolysyndactyly type 2
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Acrocephalosyndactyly type V
MONDO_0007043
FGFR2 Unknown
9973282 7655462 9002682 7874170 8696350 17621648 8528214 15523492 7607643 7719344 7581378 22038757 9677057 7987400 9152842 19610084 28425981
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Acrocephalosyndactyly type v.
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Ankylosis 1 shared geneFGFR2 Related via 1 shared gene including FGFR2. Cutis gyrata syndrome 1 shared geneFGFR2 Related via 1 shared gene including FGFR2. Antley-bixler syndrome without genital anomalies or disordered steroidogenesis 1 shared geneFGFR2 Related via 1 shared gene including FGFR2. Craniofacial-skeletal-dermatologic dysplasia, pfeiffer syndrome 1 shared geneFGFR2 Related via 1 shared gene including FGFR2. Familial scaphocephaly syndrome 1 shared geneFGFR2 Related via 1 shared gene including FGFR2.