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
Press Enter · cited answer in seconds
0 sources
STAR syndrome
Summary
STAR syndrome is a developmental defect during embryogenesis[1]. It draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).[2]
Key Facts
- STAR syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- STAR syndrome's instance of is recorded as rare disease[4].
- STAR syndrome's instance of is recorded as class of disease[5].
- STAR syndrome's subclass of is recorded as syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[6].
- STAR syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability[7].
- STAR syndrome's subclass of is recorded as syndromic anorectal malformation[8].
- STAR syndrome's subclass of is recorded as autosomal dominant disease[9].
- STAR syndrome's subclass of is recorded as syndrome[10].
- STAR syndrome's MeSH descriptor ID is recorded as C567475[11].
- STAR syndrome's OMIM ID is recorded as 300707[12].
- STAR syndrome's KEGG ID is recorded as H01156[13].
- STAR syndrome's Disease Ontology ID is recorded as DOID:0111931[14].
- STAR syndrome's Orphanet ID is recorded as 140952[15].
- STAR syndrome's health specialty is recorded as genetics[16].
- STAR syndrome's genetic association is recorded as CCNQ[17].
- STAR syndrome's Google Knowledge Graph ID is recorded as /g/11gb3n64jy[18].
- STAR syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_140952[19].
- STAR syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111931[20].
- STAR syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111931[21].
- STAR syndrome's UMLS CUI is recorded as C2678045[22].
- STAR syndrome's ICD-10-CM is recorded as Q87.8[23].
- STAR syndrome's GARD rare disease ID is recorded as 10295[24].
- STAR syndrome's Mondo ID is recorded as MONDO_0010408[25].
- STAR syndrome's ICD-11 ID is recorded as 2029143650[26].
- STAR syndrome's UniProt disease ID is recorded as DI-02373[27].
Why It Matters
STAR syndrome draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).[2]