autoimmune lymphoproliferative syndrome type 2A
autoimmune lymphoproliferative syndrome that has material basis in mutation in the CASP10 gene
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autoimmune lymphoproliferative syndrome type 2A
Summary
autoimmune lymphoproliferative syndrome type 2A is a rare disease[1].
Key Facts
- autoimmune lymphoproliferative syndrome type 2A's instance of is recorded as rare disease[2].
- autoimmune lymphoproliferative syndrome type 2A's instance of is recorded as class of disease[3].
- autoimmune lymphoproliferative syndrome type 2A is a type of autoimmune lymphoproliferative syndrome[4].
- autoimmune lymphoproliferative syndrome type 2A is a type of autosomal dominant disease[5].
- autoimmune lymphoproliferative syndrome type 2A is a type of Type 2 Autoimmune Lymphoproliferative Syndrome[6].
- autoimmune lymphoproliferative syndrome type 2A's NCI Thesaurus ID is recorded as C39576[7].
- autoimmune lymphoproliferative syndrome type 2A's genetic association is recorded as CASP10[8].
- autoimmune lymphoproliferative syndrome type 2A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110115[9].
- autoimmune lymphoproliferative syndrome type 2A's exact match is recorded as http://identifiers.org/doid/DOID:0110115[10].
- autoimmune lymphoproliferative syndrome type 2A's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].