Pfeiffer syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
PFEIFFER SYNDROME
101600C0220658MONDO:0007043
FGFR1 Causal
10945669 9586546 7719345 9002682 8841188 8434615 10394936 15523615 7874169 9150725 11807866
ClinVar, Disgenet, GWAS catalog, HPO
FGFR2 Causal
7719333 9150725 9457499 9475591 10394936 10731087 10945669 11380927 11556600 11807866
ClinGen, ClinVar, Disgenet, HPO
PFEIFFER SYNDROME TYPE 3
93260MONDO:0019661C5438850
FGFR2 Causal
20301628
GenCC, Orphanet, Disgenet
All3 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Pfeiffer syndrome.
5 View disease cluster →
Ankylosis 1 shared geneFGFR2 Related via 1 shared gene including FGFR2. Beare-stevenson cutis gyrata syndrome 1 shared geneFGFR2 Related via 1 shared gene including FGFR2. Cutis gyrata syndrome 1 shared geneFGFR2 Related via 1 shared gene including FGFR2. Osteoglophonic dysplasia 1 shared geneFGFR1 Related via 1 shared gene including FGFR1. Hartsfield-Bixler-Demyer syndrome 1 shared geneFGFR1 Related via 1 shared gene including FGFR1.