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DOID:9250 - acrocallosal syndrome
Disease Ontology Definition:A syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation.
Synonyms: ACLS, SCHINZEL ACROCALLOSAL SYNDROME, Schinzel syndrome 1
Xenbase Genes
:
sufu,
gli3,
kif7
| MONDO:0008708 - acrocallosal syndrome |
| MIM:200990 - ACROCALLOSAL SYNDROME; ACLS |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
digenic disease (is_a),
syndrome (is_a)