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AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Also Known As:
AICA Ribosuria due to ATIC Deficiency
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Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Congenital Abnormalities: 25723
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Nervous System Diseases: 14178
Neurologic Manifestations: 7102
Neurobehavioral Manifestations: 1586
Intellectual Disability: 8035
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Central Nervous System Diseases: 4213
Brain Diseases: 15694
Epilepsy: 37791
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Signs and Symptoms Pathological Conditions
Signs and Symptoms
Neurologic Manifestations: 7102
Neurobehavioral Manifestations: 1586
Intellectual Disability: 8035
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Behavior and Behavior Mechanisms
Neurobehavioral Manifestations: 1586
Intellectual Disability: 8035
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Mental Disorders: 24177
Neurodevelopmental Disorders: 3095
Intellectual Disability: 8035
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Enzymes and Coenzymes: 1
Enzymes: 152586
Transferases: 6589
One-Carbon Group Transferases
Hydroxymethyl and Formyl Transferases: 88
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Hydrolases: 2166
Aminohydrolases: 1
Nucleotide Deaminases
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency