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DOID:0111510 - Marshall syndrome
Disease Ontology Definition:An ectodermal dysplasia characterized by hypoplasia of the maxilla, nasal bones, and frontal sinuses, as well as calvarial thickening, myopia, early-onset cataracts, and sensorineural hearing loss that has_material_basis_in heterozygous or homozygous mutation (most frequently affecting splice sites) in the COL11A1 gene on chromosome 1p21.1. Mutations, typically null, in the COL11A1 gene may also cause Stickler syndrome.
Synonyms: deafness, myopia, cataract, saddle nose-Marshall type, MRSHS
Xenbase Genes
:
col11a1
| MIM:154780 - MARSHALL SYNDROME; MRSHS |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
ectodermal dysplasia (is_a)