Hyperinsulinemic hypoglycemia
Symptom Information:
| Symptom ID: | HPO:0000825 | |||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013) Abnormal glucose homeostasis(HPO:0011014) Hyperinsulinemia(HPO:0000842) Hyperinsulinemic hypoglycemia(HPO:0000825) Abnormality of the endocrine system(HPO:0000818) Abnormality of circulating hormone level(HPO:0003117) Hyperinsulinemia(HPO:0000842) Hyperinsulinemic hypoglycemia(HPO:0000825) MedDRA: |
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| Database Frequency: | 18 / 7739 | |||
| Resource: |
All diseases associated with this symptom:
| 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) |
| Beckwith-Wiedemann syndrome due to NSD1 mutation | (Orphanet:238613) |
| Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
| Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency | (Orphanet:276603) |
| Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency | (Orphanet:276598) |
| Exercise-induced hyperinsulinism | (Orphanet:165991) |
| HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4 | (OMIM:609975) |
| HYPOGLYCEMIA, LEUCINE-INDUCED | (OMIM:240800) |
| Hyperinsulinism due to INSR deficiency | (Orphanet:263458) |
| Hyperinsulinism due to glucokinase deficiency | (Orphanet:79299) |
| Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
| MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM | (OMIM:616033) |
| MPI-CDG | (Orphanet:79319) |
| Maturity-onset diabetes of the young, type 1 | (OMIM:125850) |
| PGM1-CDG | (Orphanet:319646) |