Overview
X chromosome-linked sideroblastic anemia 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.
Anemic pallor
Always present (100%)HP:0001017
Hypersideremic anemia
Always present (100%)HP:0001924
Hypochromic, microcytic anaemia
Always present (100%)HP:0004840
Ineffective erythropoiesis
Always present (100%)HP:0010972
Weakness
Always present (100%)HP:0025406
Abnormality of iron homeostasis
Very frequent (80-99%)HP:0011031
Low number of red blood cells or hemoglobin
Very frequent (80-99%)HP:0001903
Muscle weakness
Very frequent (80-99%)HP:0001324
Paleness
Very frequent (80-99%)HP:0000980
Tiredness
Very frequent (80-99%)HP:0012378
Elevated serum transaminases
Occasional (5-29%)HP:0002910
Glucose intolerance
Occasional (5-29%)HP:0001952
Large spleen
Occasional (5-29%)HP:0001744
Panting
Occasional (5-29%)HP:0002094
Patchy darkened skin
Occasional (5-29%)HP:0000953
Macrocytic anemia
HP:0001972
Related Conditions
X chromosome-linked pyridoxine responsive sideroblastic anemia(child)
X chromosome-linked pyridoxine refractory sideroblastic anemia(child)
X-linked sideroblastic anemia with spinocerebellar ataxia(child)
Sideroblastic anemia(parent)
Inherited disorder of porphyrin metabolism(parent)
Hereditary red blood cell disorder(parent)
Congenital anemia(parent)
X-linked recessive hereditary disease(parent)
Quick Facts
- SNOMED CT
- 48983004
- UMLS CUI
- C4551511
- Fully Specified Name
- X chromosome-linked sideroblastic anemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 16
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.