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Summary Literature (0)
DOID:14744 - Partington syndrome

Disease Ontology Definition:A syndrome characterized by intellectual disability, focal dystonia of the hands and dysarthria.

Synonyms: X-linked Russell-Silver syndrome

Xenbase Genes : arx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010654 - Partington syndrome

MIM:
MIM:309510 - PARTINGTON SYNDROME; PRTS

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): syndromic X-linked intellectual disability (is_a), X-linked recessive disease (is_a)