CODAS Syndrome

Alternative Names

  • Cerebral, Ocular, Dental, Auricular, And Skeletal Anomalies Syndrome
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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Other congenital malformations

OMIM Number

600373

Mode of Inheritance

Autosomal recessive

Gene Map Locus

19p13.3

Description

CODAS is an acronym for cerebral, ocular, dental, auricular, and skeletal anomalies. CODAS syndrome is a rare disorder characterized by a distinctive constellation of features that includes 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. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
600373.1Saudi ArabiaUnknownNo Developmental cataractNM_004793.4:c.44G>CHomozygousAutosomal, RecessivePatel et al. 2017
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