Add immunodeficiency 132A

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -2133,6 +2133,7 @@ Declaration(Class(obo:DOID_0061097))
 Declaration(Class(obo:DOID_0061098))
 Declaration(Class(obo:DOID_0061099))
 Declaration(Class(obo:DOID_0061100))
+Declaration(Class(obo:DOID_0061101))
 Declaration(Class(obo:DOID_0070000))
 Declaration(Class(obo:DOID_0070001))
 Declaration(Class(obo:DOID_0070002))
@@ -43583,6 +43584,17 @@ AnnotationAssertion(rdfs:label obo:DOID_0061100 "autosomal dominant primary micr
 SubClassOf(obo:DOID_0061100 obo:DOID_0070297)
 SubClassOf(obo:DOID_0061100 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
 
+# Class: obo:DOID_0061101 (immunodeficiency 132A)
+
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/36004314/") obo:IAO_0000115 obo:DOID_0061101 "A primary immunodeficiency disease that is characterized by increased susceptibility to infection with certain pathogens and that has_material_basis_in heterozygous dominant-negative mutation in the TRAF3 gene on chromosome 14q32.")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061101 "MIM:614849")
+AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0061101 "IMD132A")
+AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061101 "disease_ontology")
+AnnotationAssertion(oboInOwl:id obo:DOID_0061101 "DOID:0061101")
+AnnotationAssertion(rdfs:label obo:DOID_0061101 "immunodeficiency 132A")
+SubClassOf(obo:DOID_0061101 obo:DOID_612)
+SubClassOf(obo:DOID_0061101 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
+
 # Class: obo:DOID_0070000 (3-methylglutaconic aciduria type 8)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/27208207") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/27696117") obo:IAO_0000115 obo:DOID_0070000 "A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the HTRA2 gene on chromosome 2p13.")