Disease #06225 (MARSIS (?Marsili syndrome), OMIM:147430)

Official abbreviation MARSIS
Name ?Marsili syndrome
OMIM ID 147430
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ZFHX2
Associated tissues -
Disease features -
Remarks -

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