Harel-Yoon syndrome

Summary

DOID:0081395 - Harel-Yoon syndrome

Disease Ontology Definition:A syndrome that is characterized by delayed psychomotor development, intellectual disability, truncal hypotonia, spasticity, and peripheral neuropathy and that has_material_basis_in heterozygous mutation in the ATAD3A gene on chromosome 1p36.

Synonyms: Ocular anomalies-axonal neuropathy-developmental delay syndrome

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: atad3a

MIM:

MIM:617183 - HAREL-YOON SYNDROME; HAYOS

MIM:617183 - HAREL-YOON SYNDROME; HAYOS

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), syndrome (is_a)