Disease #05870 (SYM1A (symphalangism, proximal, type 1A (SYM1A)), OMIM:185800)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Official abbreviation	SYM1A
Name	symphalangism, proximal, type 1A (SYM1A)
OMIM ID	185800
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NOG
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-11-04 08:50:54 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.