Abnormality of the thymus
Symptom Information:
Symptom ID: | HPO:0000777 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) MedDRA: |
||
Database Frequency: | 9 / 7739 | ||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLYDEATH | (OMIM:208910) |
DIGEORGE SYNDROME | (OMIM:188400) |
Fraser syndrome | (Orphanet:2052) |
Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis | (Orphanet:137631) |
Reticular dysgenesis | (Orphanet:33355) |
Short-limb skeletal dysplasia with severe combined immunodeficiency | (Orphanet:935) |
T-B+ severe combined immunodeficiency due to gamma chain deficiency | (Orphanet:276) |
Vici syndrome | (Orphanet:1493) |