Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Childhood type dermatomyositis
Frequent (30-79%)
Dubowitz's syndrome
Occasional (5-29%)
Typhoid fever
Occasional (5-29%)
Prune belly syndrome
Frequent (30-79%)
Stiff-man syndrome
Frequent (30-79%)
Hereditary coproporphyria
Septo-optic dysplasia sequence
Occasional (5-29%)
Metaphyseal chondrodysplasia, McKusick type
Very rare (1-4%)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Always present (100%)
Caudal dysplasia sequence
Periodic disease
Very frequent (80-99%)
Russell-Silver syndrome
Frequent (30-79%)
Glucagonoma syndrome
Frequent (30-79%)
Hereditary fructosuria
Occasional (5-29%)
Nail-patella syndrome
Frequent (30-79%)
Townes syndrome
Frequent (30-79%)
Severe adrenal insufficiency
Very frequent (80-99%)
Familial dysautonomia
Congenital malrotation of intestine
Ehlers-Danlos syndrome, type 3
Frequent (30-79%)
Multiple endocrine neoplasia, type 1
Occasional (5-29%)
Holoprosencephaly sequence
Occasional (5-29%)
Thyrotoxic periodic paralysis
Frequent (30-79%)
Polymyositis
Frequent (30-79%)
Panhypopituitarism
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 14760008
- UMLS CUI
- C0009806
- Fully Specified Name
- Constipation (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.