familial cylindromatosis

Summary

familial cylindromatosis is a rare disease^[1].

Key Facts

• familial cylindromatosis's instance of is recorded as rare disease^[2].
• familial cylindromatosis's instance of is recorded as class of disease^[3].
• familial cylindromatosis's subclass of is recorded as Dermal cylindroma^[4].
• familial cylindromatosis's subclass of is recorded as Brooke-Spiegler syndrome^[5].
• familial cylindromatosis's MeSH descriptor ID is recorded as C536611^[6].
• familial cylindromatosis's OMIM ID is recorded as 132700^[7].
• familial cylindromatosis's KEGG ID is recorded as H00828^[8].
• familial cylindromatosis's Orphanet ID is recorded as 211^[9].
• familial cylindromatosis's genetic association is recorded as CYLD^[10].
• familial cylindromatosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_211^[11].
• familial cylindromatosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79493^[12].
• familial cylindromatosis's UMLS CUI is recorded as C1704217^[13].
• familial cylindromatosis's UMLS CUI is recorded as C1851526^[14].
• familial cylindromatosis's GARD rare disease ID is recorded as 9707^[15].
• familial cylindromatosis's Mondo ID is recorded as MONDO_0007565^[16].
• familial cylindromatosis's UniProt disease ID is recorded as DI-01564^[17].