STAR syndrome
This syndrome is characterised by the association of toe syndactyly, facial dysmorphism including telecanthus (abnormal distance between the eyes) and a broad nasal tip, urogenital malformations and anal atresia
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STAR syndrome
Summary
STAR syndrome is a developmental defect during embryogenesis[1].
Key Facts
- STAR syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- STAR syndrome's instance of is recorded as rare disease[3].
- STAR syndrome's instance of is recorded as class of disease[4].
- STAR syndrome is a type of syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[5].
- STAR syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[6].
- STAR syndrome is a type of syndromic anorectal malformation[7].
- STAR syndrome is a type of autosomal dominant disease[8].
- STAR syndrome is a type of syndrome[9].
- STAR syndrome's health specialty is recorded as genetics[10].
- STAR syndrome's genetic association is recorded as CCNQ[11].
- STAR syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_140952[12].
- STAR syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111931[13].
- STAR syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111931[14].