Disease #00984 (FGLDS2 (Feingold syndrome, type 2), OMIM:614326)

Official abbreviation	FGLDS2
Name	Feingold syndrome, type 2
OMIM ID	614326
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MIR17HG
Associated tissues	-
Disease features	esophageal atresias, duodenal atresias, microcephaly, learning disability, syndactyly, cardiac defect
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2026-03-24 18:51:22 +01:00 (CET)

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Global Variome shared LOVD