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Kasabach-Merritt syndrome

disorder
SNOMED 86635005CUI C0221025

Overview

Kasabach-Merritt syndrome 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.

Hemangiomata
Very frequent (80-99%)HP:0001028
Low fibrinogen level
Very frequent (80-99%)HP:0011900
Low platelet count
Very frequent (80-99%)HP:0001873
Capillary hemangioma
Frequent (30-79%)HP:0005306
Petechiae
Frequent (30-79%)HP:0000967
Red or purple spots on the skin
Frequent (30-79%)HP:0000979
Tufted hemangioma
Frequent (30-79%)HP:0012329
Abnormal lymphatic vessel morphology
Occasional (5-29%)HP:0100766
Chronic consumption coagulopathy
Occasional (5-29%)HP:0005520
Decreased haemoglobin
Occasional (5-29%)HP:0001903
Hemangioma of the liver
Occasional (5-29%)HP:0031207
Leukopenia
Occasional (5-29%)HP:0001882
Low factor II activity
Occasional (5-29%)HP:0008151
Microangiopathic hemolytic anemia
Occasional (5-29%)HP:0001937
Neutropoenia
Occasional (5-29%)HP:0001875
Profuse sweating
Occasional (5-29%)HP:0000975
Belly bloating
Very rare (1-4%)HP:0003270
Hypertrichosis
Very rare (1-4%)HP:0000998
Hypopnea
Very rare (1-4%)HP:0040213
Laboured breathing
Very rare (1-4%)HP:0002098
Reticulocytosis
Very rare (1-4%)HP:0001923
Skin cancer (non-melanoma)
Very rare (1-4%)HP:0008069
Upset stomach
Very rare (1-4%)HP:0002027
Hyperkalemia
HP:0002153
Ventricular arrhythmias
HP:0004308

Quick Facts

SNOMED CT
86635005
UMLS CUI
C0221025
Fully Specified Name
Kasabach-Merritt syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
25
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.