Brooke-Spiegler syndrome

Summary

Brooke-Spiegler syndrome is a rare disease^[1].

Key Facts

• Brooke-Spiegler syndrome's instance of is recorded as rare disease^[2].
• Brooke-Spiegler syndrome's instance of is recorded as class of disease^[3].
• Brooke-Spiegler syndrome's subclass of is recorded as autosomal dominant disease^[4].
• Brooke-Spiegler syndrome's subclass of is recorded as skin disease^[5].
• Brooke-Spiegler syndrome's OMIM ID is recorded as 605041^[6].
• Brooke-Spiegler syndrome's KEGG ID is recorded as H00827^[7].
• Brooke-Spiegler syndrome's Disease Ontology ID is recorded as DOID:0050693^[8].
• Brooke-Spiegler syndrome's Orphanet ID is recorded as 79493^[9].
• Brooke-Spiegler syndrome's genetic association is recorded as CYLD^[10].
• Brooke-Spiegler syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050693^[11].
• Brooke-Spiegler syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050693^[12].
• Brooke-Spiegler syndrome's UMLS CUI is recorded as C1857941^[13].
• Brooke-Spiegler syndrome's PatientsLikeMe condition ID is recorded as brooke-spiegler-syndrome^[14].
• Brooke-Spiegler syndrome's GARD rare disease ID is recorded as 10179^[15].
• Brooke-Spiegler syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[16].
• Brooke-Spiegler syndrome's Mondo ID is recorded as MONDO_0011512^[17].
• Brooke-Spiegler syndrome's UniProt disease ID is recorded as DI-00201^[18].