Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0080201 - Peters plus syndrome


Disease Ontology Definition:A syndrome that is characterized by anterior chamber eye anomalies, short limbs with broad distal extremities, characteristic facial features, cleft lip/palate, and variable developmental delay/intellectual disability.

Synonyms: Krause-Kivlin syndrome, Peters anomaly-short limb dwarfism syndrome, Peters-plus syndrome

Xenbase Genes : b3glct

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009856 - Peters plus syndrome

OMIM:
OMIM:261540 - PETERS-PLUS SYNDROME; PTRPLS

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): syndrome (is_a)