Statements (50)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
form of diabetes mellitus |
| gptkbp:can_be_familial |
yes
|
| gptkbp:can_be_permanent |
yes
|
| gptkbp:can_be_sporadic |
yes
|
| gptkbp:can_be_transient |
yes
|
| gptkbp:can_relapse |
yes (in transient form)
|
| gptkbp:can_remit |
yes (in transient form)
|
| gptkbp:cause |
genetic mutations
|
| gptkbp:complication |
intellectual disability
seizures developmental delay |
| gptkbp:diagnosedBy |
genetic testing
blood glucose test |
| gptkbp:differentialDiagnosis |
gptkb:type_1_diabetes_mellitus
|
| gptkbp:firstDescribed |
1950s
|
| gptkbp:gene |
gptkb:INS
KCNJ11 ABCC8 |
| gptkbp:has_onset |
within first 6 months of life
|
| https://www.w3.org/2000/01/rdf-schema#label |
Neonatal Diabetes Mellitus
|
| gptkbp:ICD-10_code |
E10-E14
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:mayPresentWith |
vomiting
respiratory distress congenital heart defects jaundice lethargy hepatomegaly macroglossia glycosuria umbilical hernia polyuria ketoacidosis intrauterine growth retardation |
| gptkbp:MeSH_ID |
D053684
|
| gptkbp:not_related_to |
autoimmune diabetes
|
| gptkbp:OMIM |
606176
|
| gptkbp:prevalence |
rare
|
| gptkbp:relatedTo |
monogenic diabetes
|
| gptkbp:riskFactor |
family history of diabetes
|
| gptkbp:symptom |
weight loss
dehydration failure to thrive hyperglycemia |
| gptkbp:treatment |
gptkb:insulin
sulfonylureas |
| gptkbp:bfsParent |
gptkb:D004053
|
| gptkbp:bfsLayer |
7
|