Aplasia of the thymus
Symptom Information:
Symptom ID: | HPO:0005359 | |||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the immune system(HPO:0002715) Abnormality of the lymphatic system(HPO:0100763) Abnormality of the thymus(HPO:0000777) Aplasia/Hypoplasia of the thymus(HPO:0010515) Aplasia of the thymus(HPO:0005359) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Thymus disorders(MedDRA:10043677) Aplasia of the thymus(HPO:0005359) |
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Database Frequency: | 6 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
DIGEORGE SYNDROME | (OMIM:188400) |
Diabetic embryopathy | (Orphanet:1926) |
Reticular dysgenesis | (Orphanet:33355) |
Severe combined immunodeficiency due to DCLRE1C deficiency | (Orphanet:275) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |