Severe combined immunodeficiency due to DCLRE1C deficiency
- Synonyms
- SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE, WITH SENSITIVITY TO IONIZING RADIATION; Severe combined immunodeficiency with sensitivity to ionizing radiation
- Modes of inheritance
- Autosomal recessive inheritance (Orphanet)
Summary
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (45 available)
Biochemical Genetics Tests
Clinical features
Help- Abnormality of head or neck
- Alopecia of scalp
Alopecia of scalp
- MedGen UID: 658454
- Concept ID: C0574769
- Finding: Finding
Abnormality of head or neck
- Oral ulcer
Oral ulcer
- MedGen UID: 57699
- Concept ID: C0149745
- Finding: Disease or Syndrome
Abnormality of head or neck
- Alopecia of scalp
- Abnormality of the digestive system
- Chronic diarrhea
Chronic diarrhea
- MedGen UID: 96036
- Concept ID: C0401151
- Finding: Finding
Abnormality of the digestive system
- Hepatomegaly
Hepatomegaly
- MedGen UID: 42428
- Concept ID: C0019209
- Finding: Finding
Abnormality of the digestive system
- Chronic diarrhea
- Abnormality of the genitourinary system
- Genital ulcers
Genital ulcers
- MedGen UID: 57716
- Concept ID: C0151281
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Genital ulcers
- Abnormality of the immune system
- Abnormally low T cell receptor excision circle level
Abnormally low T cell receptor excision circle level
- MedGen UID: 1611921
- Concept ID: C4531052
- Finding: Finding
Abnormality of the immune system
- Absent tonsils
Absent tonsils
- MedGen UID: 154366
- Concept ID: C0576999
- Finding: Finding
Abnormality of the immune system
- Aplasia of the thymus
Aplasia of the thymus
- MedGen UID: 146900
- Concept ID: C0685894
- Finding: Congenital Abnormality
Abnormality of the immune system
- B lymphocytopenia
B lymphocytopenia
- MedGen UID: 340780
- Concept ID: C1855067
- Finding: Finding
Abnormality of the immune system
- BCGitis
BCGitis
- MedGen UID: 1684722
- Concept ID: C5139070
- Finding: Disease or Syndrome
Abnormality of the immune system
- Eosinophilia
Eosinophilia
- MedGen UID: 41824
- Concept ID: C0014457
- Finding: Disease or Syndrome
Abnormality of the immune system
- Generalized lymphadenopathy
Generalized lymphadenopathy
- MedGen UID: 96909
- Concept ID: C0476486
- Finding: Finding
Abnormality of the immune system
- Increased circulating IgE concentration
Increased circulating IgE concentration
- MedGen UID: 116018
- Concept ID: C0236175
- Finding: Finding
Abnormality of the immune system
- Lymph node hypoplasia
Lymph node hypoplasia
- MedGen UID: 892318
- Concept ID: C4025683
- Finding: Finding
Abnormality of the immune system
- Lymphopenia
Lymphopenia
- MedGen UID: 7418
- Concept ID: C0024312
- Finding: Disease or Syndrome
Abnormality of the immune system
- Otitis media
Otitis media
- MedGen UID: 45253
- Concept ID: C0029882
- Finding: Disease or Syndrome
Abnormality of the immune system
- Panhypogammaglobulinemia
Panhypogammaglobulinemia
- MedGen UID: 233072
- Concept ID: C1328587
- Finding: Finding
Abnormality of the immune system
- Pneumonia
Pneumonia
- MedGen UID: 10813
- Concept ID: C0032285
- Finding: Disease or Syndrome
Abnormality of the immune system
- Sepsis
Sepsis
- MedGen UID: 48626
- Concept ID: C0036690
- Finding: Disease or Syndrome
Abnormality of the immune system
- Severe combined immunodeficiency disease
Severe combined immunodeficiency disease
- MedGen UID: 88328
- Concept ID: C0085110
- Finding: Disease or Syndrome
Abnormality of the immune system
- Splenomegaly
Splenomegaly
- MedGen UID: 52469
- Concept ID: C0038002
- Finding: Finding
Abnormality of the immune system
- Abnormally low T cell receptor excision circle level
- Abnormality of the integument
- Erythematous papule
Erythematous papule
- MedGen UID: 834002
- Concept ID: C0747241
- Finding: Finding
Abnormality of the integument
- Erythematous papule
- Abnormality of the respiratory system
- Recurrent upper respiratory tract infections
Recurrent upper respiratory tract infections
- MedGen UID: 154380
- Concept ID: C0581381
- Finding: Disease or Syndrome
Abnormality of the respiratory system
- Recurrent upper respiratory tract infections
- Growth abnormality
- Failure to thrive
Failure to thrive
- MedGen UID: 746019
- Concept ID: C2315100
- Finding: Disease or Syndrome
Growth abnormality
- Failure to thrive
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