"Galactosemias" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
Descriptor ID |
D005693
|
MeSH Number(s) |
C10.228.140.163.100.320 C16.320.565.189.320 C16.320.565.202.355 C18.452.132.100.320 C18.452.648.189.320 C18.452.648.202.355
|
Concept/Terms |
UDPglucose 4-Epimerase Deficiency Disease- UDPglucose 4-Epimerase Deficiency Disease
- UDPglucose 4 Epimerase Deficiency Disease
- Deficiency Disease, UDPglucose 4-Epimerase
- Deficiency Disease, UDPglucose 4 Epimerase
- Galactose Epimerase Deficiency
- Deficiencies, Galactose Epimerase
- Deficiency, Galactose Epimerase
- Galactose Epimerase Deficiencies
- GALE Deficiency
- Deficiencies, GALE
- Deficiency, GALE
- GALE Deficiencies
- UDP-Galactose-4-Epimerase Deficiency
- Deficiencies, UDP-Galactose-4-Epimerase
- Deficiency, UDP-Galactose-4-Epimerase
- UDP Galactose 4 Epimerase Deficiency
- UDP-Galactose-4-Epimerase Deficiencies
- UDP-Galactose-4-Epimerase Deficiency Disease
- UDP Galactose 4 Epimerase Deficiency Disease
- Galactosemia III
- Galactosemia IIIs
- Deficiency Disease, UDP-Galactose-4-Epimerase
- Deficiency Disease, UDP Galactose 4 Epimerase
- Deficiency Diseases, UDP-Galactose-4-Epimerase
- UDP-Galactose-4-Epimerase Deficiency Diseases
- Galactosemia 3
- Galactosemia 3s
Galactokinase Deficiency Disease- Galactokinase Deficiency Disease
- Galactokinase Deficiency Diseases
- Hereditary Galactokinase Deficiency
- Deficiencies, Hereditary Galactokinase
- Deficiency, Hereditary Galactokinase
- Galactokinase Deficiencies, Hereditary
- Galactokinase Deficiency, Hereditary
- Hereditary Galactokinase Deficiencies
- Galactokinase Deficiency
- Deficiencies, Galactokinase
- Deficiency, Galactokinase
- Galactokinase Deficiencies
- GALK Deficiency
- Deficiencies, GALK
- Deficiency, GALK
- GALK Deficiencies
- Deficiency Disease, Galactokinase
- Galactosemia 2
Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease- Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease
- Galactose 1 Phosphate Uridyl Transferase Deficiency Disease
- Galactose-1-Phosphate Uridyltransferase Deficiency
- Deficiencies, Galactose-1-Phosphate Uridyltransferase
- Deficiency, Galactose-1-Phosphate Uridyltransferase
- Galactose 1 Phosphate Uridyltransferase Deficiency
- Galactose-1-Phosphate Uridyltransferase Deficiencies
- Uridyltransferase Deficiencies, Galactose-1-Phosphate
- Uridyltransferase Deficiency, Galactose-1-Phosphate
- Galactose-1-Phosphate Uridylyltransferase Deficiency
- Deficiencies, Galactose-1-Phosphate Uridylyltransferase
- Deficiency, Galactose-1-Phosphate Uridylyltransferase
- Galactose 1 Phosphate Uridylyltransferase Deficiency
- Galactose-1-Phosphate Uridylyltransferase Deficiencies
- Uridylyltransferase Deficiencies, Galactose-1-Phosphate
- Uridylyltransferase Deficiency, Galactose-1-Phosphate
- GALT Deficiency
- Deficiencies, GALT
- Deficiency, GALT
- GALT Deficiencies
- UDPglucose-Hexose-1-Phosphate Uridylyltransferase Deficiency
- Deficiencies, UDPglucose-Hexose-1-Phosphate Uridylyltransferase
- Deficiency, UDPglucose-Hexose-1-Phosphate Uridylyltransferase
- UDPglucose Hexose 1 Phosphate Uridylyltransferase Deficiency
- UDPglucose-Hexose-1-Phosphate Uridylyltransferase Deficiencies
- Uridylyltransferase Deficiencies, UDPglucose-Hexose-1-Phosphate
- Uridylyltransferase Deficiency, UDPglucose-Hexose-1-Phosphate
- UTP Hexose-1-Phosphate Uridylyltransferase Deficiency
- UTP Hexose 1 Phosphate Uridylyltransferase Deficiency
- UTP-Hexose-1-Phosphate Uridylyltransferase Deficiency Disease
- UTP Hexose 1 Phosphate Uridylyltransferase Deficiency Disease
- Deficiency Disease, Galactose-1-Phosphate Uridyl-Transferase
- Deficiency Disease, Galactose 1 Phosphate Uridyl Transferase
- Galactosemia, Classic
- Classic Galactosemia
- Classic Galactosemias
- Galactosemias, Classic
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Below are MeSH descriptors whose meaning is more general than "Galactosemias".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Galactosemias [C10.228.140.163.100.320]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Galactosemias [C16.320.565.189.320]
- Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
- Galactosemias [C16.320.565.202.355]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Galactosemias [C18.452.132.100.320]
- Metabolism, Inborn Errors [C18.452.648]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Galactosemias [C18.452.648.189.320]
- Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
- Galactosemias [C18.452.648.202.355]
Below are MeSH descriptors whose meaning is more specific than "Galactosemias".
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