Hyperinsulinemia
Symptom Information:
Symptom ID: | HPO:0000842 | |||||||||||||||
Synonyms: |
|
|||||||||||||||
Quality: | ||||||||||||||||
Cross references: |
|
|||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the endocrine system(HPO:0000818) Abnormality of circulating hormone level(HPO:0003117) Hyperinsulinemia(HPO:0000842) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013) Abnormal glucose homeostasis(HPO:0011014) Hyperinsulinemia(HPO:0000842) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Glucose metabolism disorders (incl diabetes mellitus)(MedDRA:10018424) Hypoglycaemic conditions NEC(MedDRA:10021001) Hyperinsulinemia(HPO:0000842) |
|||||||||||||||
Database Frequency: | 39 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency | (Orphanet:276580) |
Autosomal dominant hyperinsulinism due to SUR1 deficiency | (Orphanet:276575) |
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency | (Orphanet:79644) |
Autosomal recessive hyperinsulinism due to SUR1 deficiency | (Orphanet:79643) |
Bangstad syndrome | (Orphanet:1227) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency | (Orphanet:276603) |
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency | (Orphanet:276598) |
Dopamine beta-hydroxylase deficiency | (Orphanet:230) |
ESTROGEN RESISTANCE | (OMIM:615363) |
Exercise-induced hyperinsulinism | (Orphanet:165991) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
HOMOZYGOUS 11p15-p14 DELETION SYNDROME | (OMIM:606528) |
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4 | (OMIM:609975) |
HYPERPROINSULINEMIA | (OMIM:616214) |
Hyperinsulinism due to glucokinase deficiency | (Orphanet:79299) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Leprechaunism | (Orphanet:508) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Perlman syndrome | (Orphanet:2849) |
Prader-Willi syndrome | (Orphanet:739) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Retinitis pigmentosa | (Orphanet:791) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |