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DOID:2962 - Cockayne syndrome
Disease Ontology Definition:A syndrome that is characterized by an abnormally small head size (microcephaly), a failure to gain weight and grow at the expected rate (failure to thrive) leading to very short stature, and delayed development.
Synonyms: Cockayne's syndrome, Neill-Dingwall syndrome
Xenbase Genes
:
ercc2,
ercc5,
ercc8,
ercc6,
ercc1
| MONDO:0016006 - Cockayne syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
syndrome (is_a)