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Dehydrated hereditary stomatocytosis

disorder
SNOMED 715526002CUI C0272051

Overview

Dehydrated 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.

Hemolytic anaemia
Very frequent (80-99%)HP:0001878
Increased red cell osmotic fragility
Very frequent (80-99%)HP:0005502
Nonspherocytic hemolytic anaemia
Very frequent (80-99%)HP:0001930
Abnormal blood K concentration
Frequent (30-79%)HP:0011042
Gallstones
Frequent (30-79%)HP:0001081
Hypochromia
Frequent (30-79%)HP:0032231
Increased ferritin
Frequent (30-79%)HP:0003281
Increased lactate dehydrogenase level
Frequent (30-79%)HP:0025435
Increased total bilirubin
Frequent (30-79%)HP:0003573
Macrocytic anemia
Frequent (30-79%)HP:0001972
Reticulocytosis
Frequent (30-79%)HP:0001923
Schistocytes
Frequent (30-79%)HP:0001981
Embolism and thrombosis
Occasional (5-29%)HP:0001907
Enlarged liver
Occasional (5-29%)HP:0002240
Episodic fatigue
Occasional (5-29%)HP:0012431
Hemoglobinuria
Occasional (5-29%)HP:0003641
Hepatitis
Occasional (5-29%)HP:0012115
Hyperbilirubinemia, neonatal
Occasional (5-29%)HP:0003265
Increased circulating hemoglobin concentration
Occasional (5-29%)HP:0001900
Increased MCV
Occasional (5-29%)HP:0005518
Increased mean corpuscular haemoglobin concentration
Occasional (5-29%)HP:0025548
Ineffective erythropoiesis
Occasional (5-29%)HP:0010972
Intermittent yellowing of skin
Occasional (5-29%)HP:0001046
Large spleen
Occasional (5-29%)HP:0001744
Neonatal hemolytic anemia
Occasional (5-29%)HP:0004804
Paleness
Occasional (5-29%)HP:0000980
Upset stomach
Occasional (5-29%)HP:0002027
Water retention
Occasional (5-29%)HP:0000969
Yellowing of the skin
Occasional (5-29%)HP:0000952
Conjunctival icterus
Very rare (1-4%)HP:0032106

Related Conditions

Autosomal dominant hereditary disorder(parent)
Erythrocyte enzyme deficiency(parent)
Stomatocytosis(parent)
Hereditary red blood cell disorder(parent)
Anemia due to membrane defect(parent)

Quick Facts

SNOMED CT
715526002
UMLS CUI
C0272051
Fully Specified Name
Dehydrated hereditary stomatocytosis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
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.