Disease #07221 (MRD75 (intellectual developmental disorder, autosomal dominant, type 75), OMIM:620988)

Official abbreviation MRD75
Name intellectual developmental disorder, autosomal dominant, type 75
OMIM ID 620988
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene DHX9
Associated tissues -
Disease features -
Remarks -
Date created 2025-12-18 16:03:37 +01:00 (CET)
Date last edited N/A

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