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.
Pallidopontonigral degeneration
Diabetes mellitus type I
Exophthalmos due to toxic diffuse goiter
Huntington's chorea
Occasional (5-29%)
Pseudohypoparathyroidism type I A
Frequent (30-79%)
Weaver syndrome
Frequent (30-79%)
Alstrom syndrome
Frequent (30-79%)
Angelman syndrome
Frequent (30-79%)
Prader-Willi syndrome
Frequent (30-79%)
Thyrotoxicosis
Kleine-Levin syndrome
Frequent (30-79%)
Craniopharyngioma
Occasional (5-29%)
Familial renal glucosuria
Frontotemporal dementia
Iodine-induced hyperthyroidism
Thyrotoxicosis with or without goiter
Graves' disease
Distal monosomy 1p36
Occasional (5-29%)
Congenital leptin deficiency
Very frequent (80-99%)
Obesity, early-onset, adrenal insufficiency, and red hair
Very frequent (80-99%)
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Occasional (5-29%)
Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency
Occasional (5-29%)
Obesity due to melanocortin 4 receptor deficiency
Very frequent (80-99%)
Pseudohypoparathyroidism type 1C
Frequent (30-79%)
2q23.1 microdeletion syndrome
Frequent (30-79%)
Related Symptoms
Quick Facts
- SNOMED CT
- 267023007
- UMLS CUI
- C0020505
- Fully Specified Name
- Excessive eating (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.