Hypoplasia of the thymus
Symptom Information:
Symptom ID: | HPO:0000778 | |||||||||||||
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) Hypoplasia of the thymus(HPO:0000778) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Thymus disorders(MedDRA:10043677) Hypoplasia of the thymus(HPO:0000778) |
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Database Frequency: | 13 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
ATAXIA-TELANGIECTASIA | (OMIM:208900) |
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
Ataxia-telangiectasia | (Orphanet:100) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
DIGEORGE SYNDROME | (OMIM:188400) |
Leprechaunism | (Orphanet:508) |
Multiple intestinal atresia | (Orphanet:2300) |
Omenn syndrome | (Orphanet:39041) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
Reticular dysgenesis | (Orphanet:33355) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Short-limb skeletal dysplasia with severe combined immunodeficiency | (Orphanet:935) |
T-B+ severe combined immunodeficiency due to gamma chain deficiency | (Orphanet:276) |