Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome

disorder

SNOMED 733064004CUI C1833792

Overview

Osteosarcoma, limb anomalies, erythroid macrocytosis 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.

Abnormality of neutrophils

Very frequent (80-99%)HP:0001874

Dental cavities

Very frequent (80-99%)HP:0000670

Increased MCV

Very frequent (80-99%)HP:0005518

Decreased body height

Frequent (30-79%)HP:0004322

Curvature of little finger

Occasional (5-29%)HP:0004209

Fused forearm bones

Occasional (5-29%)HP:0002974

Abnormal tissue mass

HP:0002664

Bone cell cancer

HP:0002669

Clinodactyly

HP:0030084

Low number of red blood cells or hemoglobin

HP:0001903

Radial deviation of finger

HP:0009466

Related Conditions

Autosomal dominant hereditary disorder(parent)

Multiple malformation syndrome with limb defect as major feature(parent)

Congenital anomaly of limb(parent)

Macrocytosis - no anemia(parent)

Osteosarcoma of bone(parent)

Hereditary disorder of musculoskeletal system(parent)

Hereditary red blood cell disorder(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 733064004
UMLS CUI: C1833792
Fully Specified Name: Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.