Disease #02540 (macrocephaly/autism syndrome, OMIM:605309)

Official abbreviation -
Name macrocephaly/autism syndrome
OMIM ID 605309
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene PTEN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00183089 - - - M no Italy - 07y - - -pp macrocephaly/autism syndrome - PTEN PTEN 1 1 Claudia Ciaccio
00458111 FamPatII1 PubMed: Graziani 2024 2-generation family, affected father/daughter F no Italy white - - yes none macrocephaly/autism syndrome macrocephaly, global developmental delay, autism, lateral ventricle dilatation - WDFY3 1 2 Ludovico Graziani
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