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

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 -

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