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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:0009856 - sac |
| MIM:261540 - PETERS-PLUS SYNDROME; PTRPLS |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)