(Q18553489)
English
Kahrizi syndrome
autosomal recessive disease that is characterized by mental retardation, cataracts, coloboma, kyphosis, and coarse facial features and has material basis in mutation in the SRD5A3 gene
- KAHRIZI SYNDROME
- Mental Retardation, Cataract, Coloboma, and Kyphosis, Autosomal Recessive
- KHRZ
- KAHRIZI SYNDROME; KHRZ
Statements
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Identifiers
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Sitelinks
Wikipedia(3 entries)
- arwiki متلازمة كهريزي
- elwiki Σύνδρομο Καχρίζι
- enwiki Kahrizi syndrome