Showing entry for Transient hypogammaglobulinemia of infancy
| General Disease Information | |
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| BXGD Id | BXGD006328 |
| Disease Name | Transient hypogammaglobulinemia of infancy |
| Disease CUI Id | C0272238 |
| MeSH Codes | C20 |
| Disease Class Name | Immune System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0001939 HP:0002715 HP:0025354 |
| Human Phenotype Ontology Term | Abnormality of metabolism/homeostasis; Abnormality of the immune system; Abnormal cellular phenotype |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations |
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