Overview
Rh deficiency 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.
Hemolytic anaemia
Very frequent (80-99%)HP:0001878
Increased red cell osmotic fragility
Very frequent (80-99%)HP:0005502
Positive direct antiglobulin test
Very frequent (80-99%)HP:0032366
Reduced haptoglobin level
Very frequent (80-99%)HP:0020181
Reticulocytosis
Very frequent (80-99%)HP:0001923
High blood bilirubin levels
Frequent (30-79%)HP:0002904
Hypochromia
Frequent (30-79%)HP:0032231
Increased lactate dehydrogenase level
Frequent (30-79%)HP:0025435
Red cell stomatocytosis
Frequent (30-79%)HP:0004446
Spherocytosis
Frequent (30-79%)HP:0004444
Anisocytosis
Occasional (5-29%)HP:0011273
Elevated heart rate
Occasional (5-29%)HP:0001649
Hepatosplenomegaly
Occasional (5-29%)HP:0001433
Hypoxemia
Occasional (5-29%)HP:0012418
Intrauterine growth retardation, IUGR
Occasional (5-29%)HP:0001511
Oligohydramnios
Occasional (5-29%)HP:0001562
Tachypnea
Occasional (5-29%)HP:0002789
Yellowing of the skin
Occasional (5-29%)HP:0000952
Macrocytic anemia
Very rare (1-4%)HP:0001972
Unconjugated hyperbilirubinemia
HP:0008282
Quick Facts
- SNOMED CT
- 37272000
- UMLS CUI
- C0272052
- Fully Specified Name
- Rh deficiency syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.