Overview
Hypogammaglobulinemia is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Bloom syndrome
Very frequent (80-99%)
Primary intestinal lymphangiectasia
Frequent (30-79%)
Metaphyseal chondrodysplasia, McKusick type
Occasional (5-29%)
Immunodeficiency with thymoma
Very frequent (80-99%)
Megaloblastic anemia due to impaired absorption of folate
Very frequent (80-99%)
Ring chromosome 21 syndrome
Occasional (5-29%)
Hypopigmentation-immunodeficiency disease
Frequent (30-79%)
Cowden syndrome
Very rare (1-4%)
Congenital defect of folate absorption
Very frequent (80-99%)
Mannosidosis
Lhermitte-Duclos disease
Very rare (1-4%)
Ataxia-telangiectasia syndrome
Very frequent (80-99%)
Radial aplasia-thrombocytopenia syndrome
Multiple myeloma (clinical)
Frequent (30-79%)
Reticular dysgenesis
Very frequent (80-99%)
Deficiency of alpha-mannosidase
Major histocompatibility complex class II deficiency
Frequent (30-79%)
Hennekam lymphangiectasia-lymphoedema syndrome
Very frequent (80-99%)
WHIM - Warts, hypogammaglobulinaemia, infections and myelokathexis
Frequent (30-79%)
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
Very frequent (80-99%)
TCN2 - Transcobalamin II deficiency
Frequent (30-79%)
Primary Sjogren's syndrome
Occasional (5-29%)
Dowling-Meara epidermolysis bullosa
Occasional (5-29%)
N-Acetylglucosaminyl transferase II deficiency
Occasional (5-29%)
Lysinuric protein intolerance
Very rare (1-4%)
Quick Facts
- SNOMED CT
- 119250001
- UMLS CUI
- C0086438
- Fully Specified Name
- Hypogammaglobulinemia (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.