Overview
Hereditary thrombocytopenic disorder is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Radial aplasia-thrombocytopenia syndrome(child)
Bernard Soulier syndrome(child)
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type(child)
Wiskott-Aldrich syndrome(child)
Fanconi pancytopenia syndrome(child)
DK phocomelia syndrome(child)
Autosomal dominant macrothrombocytopenia(child)
X-linked congenital dyserythropoietic anemia with thrombocytopenia(child)
Thyrocerebrorenal syndrome(child)
Hereditary thrombocytopenia with normal platelets(child)
X-linked thrombocytopenia with normal platelets(child)
DIAPH1-related sensorineural deafness, thrombocytopenia syndrome(child)
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome(child)
Hereditary thrombocytopenia with early-onset myelofibrosis(child)
Autosomal dominant thrombocytopenia with platelet secretion defect(child)
Severe autosomal recessive macrothrombocytopenia(child)
Congenital autosomal recessive small-platelet thrombocytopenia(child)
Lazy leukocyte syndrome(child)
Autosomal recessive combined immunodeficiency due to WIPF1 mutation(child)
Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect(child)
Quick Facts
- SNOMED CT
- 438492008
- UMLS CUI
- C2586012
- Fully Specified Name
- Hereditary thrombocytopenic disorder (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.