Disease #06127 (IDDMSSD (Intellectual developmental disorder with macrocephaly, seizures, and speech delay), OMIM:618158)

Official abbreviation IDDMSSD
Name Intellectual developmental disorder with macrocephaly, seizures, and speech delay
OMIM ID 618158
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PAK1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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