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CODAS syndrome

Disease Summary
Associated Targets (1)
Tbio

1


Explore Associated Targets
Mondo Description Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies.
Uniprot Description A rare syndrome characterized by the combination of cerebral, ocular, dental, auricular, and skeletal features. These include developmental delay, craniofacial anomalies, cataracts, ptosis, median nasal groove, delayed tooth eruption, hearing loss, short stature, delayed epiphyseal ossification, metaphyseal hip dysplasia, and vertebral coronal clefts.
Mondo Term and Equivalent IDs
MONDO:0010879:  CODAS syndrome
DOID:0111274: 
GARD:0001418: 
MESH:C536434: 
NCIT:C126744: 
Orphanet:1458: 
SCTID:717772000: 
UMLS:C1838180: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)