Overview
Congenital thrombocytopenia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Wiskott-Aldrich syndrome(child)
Radial aplasia-thrombocytopenia syndrome(child)
Amegakaryocytic thrombocytopenia with congenital malformation(child)
Stormorken syndrome(child)
Congenital amegakaryocytic thrombocytopenia(child)
DK phocomelia syndrome(child)
Autosomal dominant macrothrombocytopenia(child)
X-linked congenital dyserythropoietic anemia with thrombocytopenia(child)
Thyrocerebrorenal syndrome(child)
Constitutional aplastic anemia(child)
Kasabach-Merritt syndrome(child)
Bleeding diathesis due to thromboxane synthesis deficiency(child)
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome(child)
Congenital autosomal recessive small-platelet thrombocytopenia(child)
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome(child)
MYH9 related disease(child)
Autosomal recessive combined immunodeficiency due to WIPF1 mutation(child)
Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect(child)
Congenital disease(parent)
Thrombocytopenic disorder(parent)
Quick Facts
- SNOMED CT
- 737221003
- UMLS CUI
- C0272278
- Fully Specified Name
- Congenital thrombocytopenia (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.