Severe T-cell immunodeficiency

Symptom Information:

Symptom ID: HPO:0005352
Synonyms:
Cellular immune deficiency [Orphanet:47320]
T-lymphocyte deficiency (finding) [Orphanet:47320]
T-lymphocyte deficiency [Orphanet:47320]
Severe T-cell immunodeficiency [OMIM:Severe T-cell immunodeficiency]
T-cell deficiency/cellular immunity deficiency [Orphanet:47320]
T-lymphocyte deficiency [OMIM:T-lymphocyte deficiency]
Quality:
Cross references:
HPO:0005354 "Absent cellular immunity" [Orphanet:47320]
HPO:0005374 "Cellular immunodeficiency" [Orphanet:47320]
HPO:0002843 "Abnormality of T cells" [Orphanet:47320]
Orphanet:47320 "T-cell deficiency/cellular immunity deficiency" [Orphanet:47320]
OMIM: "Severe T-cell immunodeficiency" [OMIM:Severe T-cell immunodeficiency]
OMIM: "T-lymphocyte deficiency" [OMIM:T-lymphocyte deficiency]
UMLS:C1744558 "T-lymphocyte deficiency" [Orphanet:47320]
Is a (Direct Parents):
Orphanet Recurrent bacterial infections
HPO         Cellular immunodeficiency
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:
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)