macrocephaly-autism syndrome

Summary
Synonym
  • macrocephaly-intellectual disability-autism syndrome
Definition
A syndrome characterized by macrocephaly, facial phenotypes including square outline with frontal bossing, 'dished-out' midface, biparietal narrowing, and long philtrum, developmental delay and autism that has_material_basis_in heterozygous mutation in the PTEN gene on chromosome 10q23.
Super Class
autosomal dominant disease syndrome
Disease Ontology
DOID:0060867
Mondo Disease Ontology
MeSH
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5728 PTEN phosphatase and tensin homolog
The Human Phenotype Ontology
Displaying entries 31 - 40 of 49 in total
HPO ID HPO Term
HP:0001263 Global developmental delay
HP:0000286 Epicanthus
HP:0001888 Lymphopenia
HP:0004422 Biparietal narrowing
HP:0011220 Prominent forehead
HP:0001513 Obesity
HP:0000717 Autism
HP:0002719 Recurrent infections
HP:0000218 High palate
HP:0001744 Splenomegaly
Displaying 1 entry
Gene ID Gene Symbol Description
5728 PTEN phosphatase and tensin homolog

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024