Hyperinsulinemia

Symptom Information:

Symptom ID: HPO:0000842
Synonyms:
Elevated insulin level [HPO:0000842]
Hyperinsulinism [Orphanet:41690]
Hyperinsulinism (disorder) [Orphanet:41690]
Hyperinsulinaemia [HPO:0000842]
Hyperinsulinemia [OMIM:Hyperinsulinemia]
Hyperinsulinism/hyperinsulinemia [Orphanet:41690]
Hyperinsulinaemia [Orphanet:41690]
Hyperinsulinaemia [MedDRA:10060378]
Hyperinsulinemia [MedDRA:10060378]
Hyperinsulinism [MedDRA:10061211]
Hyperinsulinism NOS [MedDRA:10061211]
Hyperinsulinism, other [MedDRA:10061211]
Other hyperinsulinism [MedDRA:10061211]
Hyperinsulinemia (in male patient) [OMIM:Hyperinsulinemia (in male patient)]
Hyperinsulinism [OMIM:Hyperinsulinism]
Quality:
Cross references:
Orphanet:41690 "Hyperinsulinism/hyperinsulinemia" [Orphanet:41690]
OMIM: "Hyperinsulinemia" [OMIM:Hyperinsulinemia]
OMIM: "Hyperinsulinemia (in male patient)" [OMIM:Hyperinsulinemia (in male patient)]
OMIM: "Hyperinsulinism" [OMIM:Hyperinsulinism]
UMLS:C0020459 "Hyperinsulinaemia" [HPO:0000842]
UMLS:C0020459 "Hyperinsulinism" [Orphanet:41690]
Is a (Direct Parents):
HPO         Abnormality of circulating hormone level
MedDRA Hypoglycaemic conditions NEC
Orphanet Diabetes mellitus
HPO         Abnormal glucose homeostasis
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)