Tatton-Brown–Rahman syndrome

Summary

Tatton-Brown–Rahman syndrome is a syndrome^[1]. It draws 7 Wikipedia views per month (syndrome category, ranking #54 of 65).^[2]

Key Facts

• Tatton-Brown–Rahman syndrome's instance of is recorded as syndrome^[3].
• Tatton-Brown–Rahman syndrome's instance of is recorded as developmental defect during embryogenesis^[4].
• Tatton-Brown–Rahman syndrome's instance of is recorded as rare disease^[5].
• Tatton-Brown–Rahman syndrome's instance of is recorded as overgrowth syndrome^[6].
• Nazneen Rahman is named after Tatton-Brown–Rahman syndrome^[7].
• Tatton-Brown–Rahman syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability^[8].
• Tatton-Brown–Rahman syndrome's subclass of is recorded as genetic syndromic intellectual disability^[9].
• Tatton-Brown–Rahman syndrome's OMIM ID is recorded as 615879^[10].
• Tatton-Brown–Rahman syndrome's KEGG ID is recorded as H02294^[11].
• Tatton-Brown–Rahman syndrome's Orphanet ID is recorded as 404443^[12].
• Tatton-Brown–Rahman syndrome's genetic association is recorded as DNMT3A^[13].
• Tatton-Brown–Rahman syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_404443^[14].
• Tatton-Brown–Rahman syndrome's UMLS CUI is recorded as C4014545^[15].
• Tatton-Brown–Rahman syndrome's ICD-10-CM is recorded as Q87.3^[16].
• Tatton-Brown–Rahman syndrome's Mondo ID is recorded as MONDO_0014382^[17].
• Tatton-Brown–Rahman syndrome's UniProt disease ID is recorded as DI-04151^[18].

Why It Matters

Tatton-Brown–Rahman syndrome draws 7 Wikipedia views per month (syndrome category, ranking #54 of 65).^[2]