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Phagocytic cell dysfunction

MONDO:0024627

Also 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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Where it sits in the disease tree

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Part of

↑ Immune system disorder (12993)

Sub-types of Phagocytic cell dysfunction

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
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 →
Phagocyte bactericidal dysfunction 0 trials · 37 incl. sub-types
1 sub-type
- Chronic granulomatous disease 37 trials Sub-types →
Defective phagocytic cell chemotaxis 0 trials
Defective phagocytic cell opsonization 0 trials
Familial lipochrome histiocytosis 0 trials
Phagocytosis, plasma-related defect 1N 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)

Including sub-types (77) Tagged with Phagocytic cell dysfunction (1)

Trials to join now! 33 Not yet recruiting 3 Not yet finished but already full! 29 Completed 10 Terminated 2