loading...| Preferred Name | Galactosemia | |
| Synonyms |
Galactosemia |
|
| Definitions |
An autosomal recessive inherited metabolic disorder caused by mutations in the GALE, GALK1, and GALT genes. It is characterized by deficiency of the enzymes responsible for the metabolism of galactose. Signs and symptoms include intellectual disability, hepatomegaly, hepatic failure, and renal failure. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84723 |
|
| code |
C84723 |
|
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842 |
|
| Contributing_Source |
Cellosaurus NICHD |
|
| DEFINITION |
An autosomal recessive inherited metabolic disorder caused by mutations in the GALE, GALK1, and GALT genes. It is characterized by deficiency of the enzymes responsible for the metabolism of galactose. Signs and symptoms include intellectual disability, hepatomegaly, hepatic failure, and renal failure. |
|
| FULL_SYN |
Galactosemia |
|
| label |
Galactosemia |
|
| Preferred_Name |
Galactosemia |
|
| prefixIRI |
Thesaurus:C84723 |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C0016952 |
|
| subClassOf |