Severe T-cell immunodeficiency
Symptom Information:
Symptom ID: | HPO:0005352 | |||||||
Synonyms: |
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Cross references: |
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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 immune system physiology(HPO:0010978) Immunodeficiency(HPO:0002721) Cellular immunodeficiency(HPO:0005374) Severe T-cell immunodeficiency(HPO:0005352) MedDRA: |
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Database Frequency: | 20 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Ataxia-telangiectasia | (Orphanet:100) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
CHARGE syndrome | (Orphanet:138) |
Cernunnos-XLF deficiency | (Orphanet:169079) |
Combined immunodeficiency T+ B+ due to partial RAG1 deficiency | (Orphanet:231154) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
Dyskeratosis congenita | (Orphanet:1775) |
Fraser syndrome | (Orphanet:2052) |
Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
ICF syndrome | (Orphanet:2268) |
Primary immunodeficiency syndrome due to p14 deficiency | (Orphanet:90023) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Reticular dysgenesis | (Orphanet:33355) |
Sanjad-Sakati syndrome | (Orphanet:2323) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy | (Orphanet:169095) |
Short-limb skeletal dysplasia with severe combined immunodeficiency | (Orphanet:935) |
Vici syndrome | (Orphanet:1493) |
X-linked lymphoproliferative disease | (Orphanet:2442) |