Temple-Baraitser syndrome

Summary

Temple-Baraitser syndrome is a developmental defect during embryogenesis^[1]. It draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]

Key Facts

• Temple-Baraitser syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Temple-Baraitser syndrome's instance of is recorded as rare disease^[4].
• Temple-Baraitser syndrome's instance of is recorded as class of disease^[5].
• Temple-Baraitser syndrome's subclass of is recorded as syndromic nail anomaly^[6].
• Temple-Baraitser syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability^[7].
• Temple-Baraitser syndrome's subclass of is recorded as genetic syndromic intellectual disability^[8].
• Temple-Baraitser syndrome's MeSH descriptor ID is recorded as C567516^[9].
• Temple-Baraitser syndrome's OMIM ID is recorded as 611816^[10].
• Temple-Baraitser syndrome's Orphanet ID is recorded as 420561^[11].
• Temple-Baraitser syndrome's genetic association is recorded as KCNH1^[12].
• Temple-Baraitser syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_420561^[13].
• Temple-Baraitser syndrome's UMLS CUI is recorded as C2678486^[14].
• Temple-Baraitser syndrome's ICD-10-CM is recorded as Q87.2^[15].
• Temple-Baraitser syndrome's GARD rare disease ID is recorded as 9441^[16].
• Temple-Baraitser syndrome's Mondo ID is recorded as MONDO_0012735^[17].
• Temple-Baraitser syndrome's UniProt disease ID is recorded as DI-04297^[18].

Why It Matters

Temple-Baraitser syndrome draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]