Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal circulating C-peptide concentration
Frequent (30-79%)HP:0030794
Abnormal circulating insulin concentration
Frequent (30-79%)HP:0040214
Abnormal glucose tolerance
Frequent (30-79%)HP:0001952
Abnormal oral glucose tolerance
Frequent (30-79%)HP:0004924
Elevated glycated haemoglobin
Frequent (30-79%)HP:0040217
Glucose in urine
Frequent (30-79%)HP:0003076
Hyperglycemia
Frequent (30-79%)HP:0003074
Hypoinsulinemia
Frequent (30-79%)HP:0040216
Fetal macrosomia
Occasional (5-29%)HP:0001520
Hyperinsulinemia hypoglycemia
Occasional (5-29%)HP:0000825
Insulin-resistant diabetes
Occasional (5-29%)HP:0000831
Intrauterine growth retardation, IUGR
Occasional (5-29%)HP:0001511
Kidney damage
Occasional (5-29%)HP:0000112
Neonatal hypoglycemia
Occasional (5-29%)HP:0001998
Noninflammatory retina disease
Occasional (5-29%)HP:0000488
Overweight
Occasional (5-29%)HP:0025502
Transient neonatal diabetes mellitus
Occasional (5-29%)HP:0008255
Genitourinary disease
Very rare (1-4%)HP:0000119
Hepatic adenoma
Very rare (1-4%)HP:0012028
Hypoplastic pancreas
Very rare (1-4%)HP:0002594
Obesity
Very rare (1-4%)HP:0001513
Pancreatic insufficiency
Very rare (1-4%)HP:0001738
Renal anomalies
Very rare (1-4%)HP:0000077
Renal cyst
Very rare (1-4%)HP:0000107
Flushing
HP:0031284
Maturity onset diabetes of the young
HP:0004904
Related Conditions
Diabetes mellitus autosomal dominant type II(child)
Maturity onset diabetes of the young, type 1(child)
Maturity-onset diabetes of the young, type 3(child)
Maturity-onset diabetes of the young, type 4(child)
Maturity-onset diabetes of the young, type 5(child)
Maturity-onset diabetes of the young, type 6(child)
Maturity-onset diabetes of the young, type 7(child)
Diabetes-pancreatic exocrine dysfunction syndrome(child)
Maturity-onset diabetes of the young, type 9(child)
Maturity-onset diabetes of the young, type 10(child)
Maturity-onset diabetes of the young, type 11(child)
Diabetes mellitus due to genetic defect in beta cell function(parent)
Genetic disease(parent)
Quick Facts
- SNOMED CT
- 609561005
- UMLS CUI
- C0342276
- Fully Specified Name
- Maturity-onset diabetes of the young (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 26
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.