PASLI Disease

Summary

PASLI Disease is a rare disease^[1].

Key Facts

• PASLI Disease's instance of is recorded as rare disease^[2].
• PASLI Disease's instance of is recorded as class of disease^[3].
• PASLI Disease's subclass of is recorded as autosomal dominant disease^[4].
• PASLI Disease's subclass of is recorded as combined immunodeficiency^[5].
• PASLI Disease's said to be the same as is recorded as activated PI3K delta syndrome^[6].
• PASLI Disease's OMIM ID is recorded as 616005^[7].
• PASLI Disease's Disease Ontology ID is recorded as DOID:0111949^[8].
• PASLI Disease's NCI Thesaurus ID is recorded as C176703^[9].
• PASLI Disease's health specialty is recorded as medical genetics^[10].
• PASLI Disease's genetic association is recorded as PIK3R1^[11].
• PASLI Disease's genetic association is recorded as PIK3CD^[12].
• PASLI Disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_397596^[13].
• PASLI Disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111949^[14].
• PASLI Disease's exact match is recorded as http://identifiers.org/doid/DOID:0111949^[15].
• PASLI Disease's UMLS CUI is recorded as C4014934^[16].
• PASLI Disease's GARD rare disease ID is recorded as 11983^[17].
• PASLI Disease's Mondo ID is recorded as MONDO_0014453^[18].
• PASLI Disease's Microsoft Academic ID is recorded as 2776141744^[19].