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Familial platelet syndrome with predisposition to acute myelogenous leukemia
disorderSNOMED 725034002CUI C1832388
Overview
Familial platelet syndrome with predisposition to acute myelogenous leukemia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal dense granule content
Always present (100%)HP:0012529
Acute monocytic leukaemia
Always present (100%)HP:0004845
Blood spots
Always present (100%)HP:0000979
Ecchymosis
Always present (100%)HP:0031364
Impaired ADP-induced platelet aggregation
Always present (100%)HP:0004866
Impaired arachidonic acid-induced platelet aggregation
Always present (100%)HP:0011870
Impaired collagen-induced platelet aggregation
Always present (100%)HP:0008320
Impaired platelet aggregation
Always present (100%)HP:0003540
Increased bleeding time
Always present (100%)HP:0003010
Low platelet count
Always present (100%)HP:0001873
Petechiae
Always present (100%)HP:0000967
Acute myeloid leukaemia
Occasional (5-29%)HP:0004808
Abnormal alpha granule content
HP:0012527
Abnormal platelet shape
Excluded (<1%)HP:0012524
Bruising susceptibility
HP:0000978
Cancer of early nerve cells
HP:0003006
Cancer of lymphatic system
HP:0002665
Hypoplastic myelodysplasia
HP:0002863
Nasal hemorrhage
HP:0000421
Quick Facts
- SNOMED CT
- 725034002
- UMLS CUI
- C1832388
- Fully Specified Name
- Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 19
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.