ZFIN Human Disease: acrocephalosyndactylia

OBO ID: DOID:12960

Term Name:	acrocephalosyndactylia		Search Ontology:
Synonyms:	Apert syndrome
Definition:	A synostosis that results_in craniosynostosis and syndactyly. http://en.wikipedia.org/wiki/Acrocephalosyndactylia
References:	ICD9CM:755.55 MESH:D000168 NCI:C34348 OMIM:101200 SNOMEDCT_US_2023_03_01:63661009 UMLS_CUI:C1510455
Ontology:	Human Disease ( DOID:12960 )

Relationships

is a type of:	synostosis synostosis Show first 5 Terms
has subtype:	Carpenter syndrome Greig cephalopolysyndactyly syndrome Pfeiffer syndrome Saethre-Chotzen syndrome Sakati-Nyhan syndrome Carpenter syndrome Greig cephalopolysyndactyly syndrome Pfeiffer syndrome Saethre-Chotzen syndrome Sakati-Nyhan syndrome Show first 5 Terms

OTHER acrocephalosyndactylia PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FGFR2	fgfr2	Apert syndrome	101200

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None