Overview
Underweight 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.
Subacute neuronopathic Gaucher's disease
Coffin-Lowry syndrome
Schwartz-Jampel syndrome
Occasional (5-29%)
Xeroderma pigmentosum, group F
Occasional (5-29%)
Marshall-Smith syndrome
Always present (100%)
Leprechaunism syndrome
Frequent (30-79%)
Ring chromosome 11 syndrome
Frequent (30-79%)
Merosin deficient congenital muscular dystrophy
Occasional (5-29%)
Abdominal cutaneous nerve entrapment syndrome
Very rare (1-4%)
Insulin resistance - type B
Frequent (30-79%)
Diencephalic syndrome
Very frequent (80-99%)
Succinyl-CoA acetoacetate transferase deficiency
Occasional (5-29%)
Eichsfeld type congenital muscular dystrophy
Very frequent (80-99%)
Congenital myotonic dystrophy
Occasional (5-29%)
Wolcott-Rallison dysplasia
Frequent (30-79%)
Peters plus syndrome
Ohdo syndrome, Maat-Kievit-Brunner type
Occasional (5-29%)
Microphthalmia, cataract, radiculomegaly and septal heart defect
Occasional (5-29%)
Christianson syndrome
FOXG1 syndrome
Frequent (30-79%)
Methyl-CpG (cytosine phosphate guanine) binding protein-2 duplication syndrome
Always present (100%)
Congenital reticular ichthyosiform erythroderma
Always present (100%)
Mowat-Wilson syndrome
Frequent (30-79%)
Growth delay due to insulin-like growth factor I resistance
Atypical Werner syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 248342006
- UMLS CUI
- C0041667
- Fully Specified Name
- Underweight (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.