Xerocytosis

disorder

SNOMED 87994004CUI C0272051

Overview

Xerocytosis 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

Hyperferritinemia

Frequent (30-79%)HP:0003281

Hypochromia

Frequent (30-79%)HP:0032231

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

Congenital hemolytic anemia

Occasional (5-29%)HP:0004804

Edema

Occasional (5-29%)HP:0000969

Embolism and thrombosis

Occasional (5-29%)HP:0001907

Enlarged liver

Occasional (5-29%)HP:0002240

Episodic fatigue

Occasional (5-29%)HP:0012431

Gastro pain

Occasional (5-29%)HP:0002027

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

Paleness

Occasional (5-29%)HP:0000980

Yellowing of the skin

Occasional (5-29%)HP:0000952

Conjunctival icterus

Very rare (1-4%)HP:0032106

Related Conditions

Anaemia due to intrinsic red cell abnormality(parent)

Quick Facts

SNOMED CT: 87994004
UMLS CUI: C0272051
Fully Specified Name: Xerocytosis (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.