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Echinobase
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

Echinobase Genes : b3glct


MIM:
MIM:261540 - peters-plus syndrome

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

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