Disease #00526 (Pfeiffer (Pfeiffer syndrome), OMIM:101600)

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Official abbreviation	Pfeiffer
Name	Pfeiffer syndrome
OMIM ID	101600
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	FGFR1, FGFR2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-16 21:40:49 +02:00 (CEST)
Date last edited	N/A