FRUCTOSE AND GALACTOSE INTOLERANCE

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr:
OMIM Id: 229500
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal recessive inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0001250) Seizures 1245 / 7739
2
 (HPO:0005973) Fructose intolerance 2 / 7739
3
 (HPO:0001943) Hypoglycemia 131 / 7739
4
 (HPO:0004919) Galactose intolerance 1 / 7739
5
 (OMIM) Galactose-induced hypoglycemia 1 / 7739
6
 (OMIM) High serum insulin by immunoassay 1 / 7739
7
 (OMIM) Fructose-induced hypoglycemia 1 / 7739
8
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739
9
 (OMIM) Normal Galactose-1-phosphate uridyl transferase 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: