Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | ACAD8 CL E G H | 27034 | 87 | ORPHA:79159 | Isobutyryl-CoA dehydrogenase deficiency | HP:0040283 - Occasional | | | 58 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | ACADS CL E G H | 35 | 90 | ORPHA:26792 | Short chain acyl-CoA dehydrogenase deficiency | HP:0040283 - Occasional | | | 90 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | GYS2 CL E G H | 2998 | 4707 | ORPHA:2089 | Glycogen storage disease due to hepatic glycogen synthase deficiency | HP:0040282 - Frequent | | | 100 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | HNF1A CL E G H | 6927 | 11621 | ORPHA:324575 | Hyperinsulinism due to HNF1A deficiency | HP:0040283 - Occasional | | | 161 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | MC2R CL E G H | 4158 | 6930 | ORPHA:361 | Familial glucocorticoid deficiency | HP:0040281 - Very frequent | | | 94 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | MRAP CL E G H | 56246 | 1304 | ORPHA:361 | Familial glucocorticoid deficiency | HP:0040281 - Very frequent | | | 26 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | NNT CL E G H | 23530 | 7863 | ORPHA:361 | Familial glucocorticoid deficiency | HP:0040281 - Very frequent | | | 13 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | PHKB CL E G H | 5257 | 8927 | ORPHA:79240 | Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency | | | | 101 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | SLC16A1 CL E G H | 6566 | 10922 | OMIM:616095 | Monocarboxylate transporter 1 deficiency | . | | | 74 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | STAR CL E G H | 6770 | 11359 | ORPHA:361 | Familial glucocorticoid deficiency | HP:0040281 - Very frequent | | | 45 | | |
HP:0012734 | HP:0012734 | Ketotic hypoglycemia | 0 | TXNRD2 CL E G H | 10587 | 18155 | ORPHA:361 | Familial glucocorticoid deficiency | HP:0040281 - Very frequent | | | 85 | | |