Disease #00055 (BLAUS (BLAU SYNDROME), OMIM:186580)

MVZ für Humangenetik Regensburg

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Official abbreviation	BLAUS
Name	BLAU SYNDROME
OMIM ID	186580
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NOD2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-10-08 10:47:22 +00:00 (UTC)
Date last edited	2023-06-16 09:49:52 +00:00 (UTC)