Overview
Pale complexion is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Hemolytic anemia due to warm antibody
Very frequent (80-99%)
Hemoglobin Bart's hydrops syndrome
Very frequent (80-99%)
Hereditary persistence of fetal hemoglobin thalassemia
Very frequent (80-99%)
Cyclical vomiting syndrome
Atopic dermatitis
Congenital atresia of esophagus
Occasional (5-29%)
Congenital dyserythropoietic anemia, type III
Occasional (5-29%)
Homozygous beta thalassemia
Very frequent (80-99%)
Megaloblastic anemia due to impaired absorption of folate
Very frequent (80-99%)
Fructose-biphosphatase deficiency
Occasional (5-29%)
Panhypopituitarism
Frequent (30-79%)
Idiopathic pulmonary hemosiderosis
Frequent (30-79%)
Congenital heart block
Occasional (5-29%)
Von Hippel-Lindau syndrome
Occasional (5-29%)
X chromosome-linked sideroblastic anemia
Very frequent (80-99%)
Goodpasture's syndrome
Frequent (30-79%)
Childhood absence epilepsy
Frequent (30-79%)
Myelofibrosis
Frequent (30-79%)
Hereditary spherocytosis
Frequent (30-79%)
Rheumatic fever
Frequent (30-79%)
Multiple endocrine neoplasia, type 2
Frequent (30-79%)
Congenital defect of folate absorption
Very frequent (80-99%)
Beta thalassemia
Very frequent (80-99%)
Hemoglobin D disease
Very rare (1-4%)
Aase syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 398979000
- UMLS CUI
- C0241137
- Fully Specified Name
- Pale complexion (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.