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Overhydrated hereditary stomatocytosis

disorder
SNOMED 722125003CUI C1861455

Overview

Overhydrated hereditary stomatocytosis 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 erythrocyte volume
Very frequent (80-99%)HP:0025065
Decreased mean corpuscular haemoglobin
Very frequent (80-99%)HP:0025547
Hemolytic anaemia
Very frequent (80-99%)HP:0001878
Increased red cell osmotic fragility
Very frequent (80-99%)HP:0005502
Red cell stomatocytosis
Very frequent (80-99%)HP:0004446
Reticulocytosis
Very frequent (80-99%)HP:0001923
Blood clot in artery of lung
Frequent (30-79%)HP:0002204
Yellowing of the skin
Frequent (30-79%)HP:0000952
Abnormal thrombosis
Occasional (5-29%)HP:0001977
Anisocytosis
Occasional (5-29%)HP:0011273
Increased lactate dehydrogenase level
Occasional (5-29%)HP:0025435
Increased MCV
Occasional (5-29%)HP:0005518
Intermittent yellowing of skin
Occasional (5-29%)HP:0001046
Large spleen
Occasional (5-29%)HP:0001744
Prolonged neonatal jaundice
Occasional (5-29%)HP:0006579
Tiredness
Occasional (5-29%)HP:0012378
Enlarged liver
HP:0002240
High blood bilirubin levels
HP:0002904
Increased intracellular Na+ levels
HP:0003575

Quick Facts

SNOMED CT
722125003
UMLS CUI
C1861455
Fully Specified Name
Overhydrated hereditary stomatocytosis (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.