Phagocytic cell dysfunction
MONDO:0024627Also known as: defective phagocytosis, phagocytic cell dysfunction
77 clinical trials for this condition and its sub-types, 1 tagged with Phagocytic cell dysfunction itself.
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Sub-types of Phagocytic cell dysfunction
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Langerhans cell histiocytosis 40 trials · 41 incl. sub-types
8 sub-types
- Langerhans cell histiocytosis specific to childhood 1 trial Sub-types →
- Langerhans cell histiocytosis specific to adulthood 0 trials Sub-types →
- Eosinophilic granuloma 0 trials Sub-types →
- Hand-Schuller-Christian disease 0 trials
- Multisystem langerhans cell histiocytosis 0 trials
- Pulmonary langerhans cell histiocytosis 0 trials
- Single-system multifocal langerhans cell histiocytosis 0 trials
- Unifocal langerhans cell histiocytosis 0 trials
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Defective phagocytic cell engulfment 0 trials · 37 incl. sub-types
5 sub-types
- Chronic granulomatous disease 37 trials Sub-types →
- Inherited glutathione synthetase deficiency 1 trial Sub-types →
- Myeloperoxidase deficiency 1 trial
- Gluthathione peroxidase deficiency 0 trials
- Specific granule deficiency 0 trials Sub-types →
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Phagocyte bactericidal dysfunction 0 trials · 37 incl. sub-types
1 sub-type
- Chronic granulomatous disease 37 trials Sub-types →
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Defective phagocytic cell chemotaxis 0 trials
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Familial lipochrome histiocytosis 0 trials
Most studied deeper sub-types
Granulomatous disease, chronic, X-linked
(10)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1
(3)
Glutathione synthetase deficiency with 5-oxoprolinuria
(1)
Adult pulmonary Langerhans cell histiocytosis
(0)
Glutathione synthetase deficiency without 5-oxoprolinuria
(0)
Granulomatous disease, chronic, autosomal recessive, 5
(0)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
(0)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
(0)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3
(0)
Granulomatous disease with defect in neutrophil chemotaxis
(0)
Hashimoto-Pritzker syndrome
(0)
Letterer-Siwe disease
(0)
Specific granule deficiency 1
(0)
Specific granule deficiency 2
(0)