
PathWhiz ID | Pathway | Meta Data |
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PW064723 |
disease
CancerBacteria
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Creator: Guest: Anonymous Created On: April 21, 2018 at 19:06 Last Updated: April 21, 2018 at 19:06 |
PW000093 |
disease
Canavan DiseaseHomo sapiens
Canavan Disease (Canavan-Van Bogaert-Bertrand Disease; Aminoacylase 2 Deficiency; Spongy Degeneration of the Central Nervous System; Aspartoacylase Deficiency; ASP Deficiency; ACY2 Deficiency; ASPA) is a rare autosomal recessive disease caused by a defect in the ASPA gene which codes for aspartoacylase. A deficiency in this enzyme results in accumulation of N-Acetyl-L-aspartic acid in plasma, spinal fluid, and urine. Symptoms, which present at birth, include myclonus, irritability, hypotonia, motor retardation, and poor head control. The neurological complications are due to demyelination of neurons and leukodystrophy. Premature death often results, though lithium citrate can be used as a treatment.
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Creator: WishartLab Created On: August 01, 2013 at 15:52 Last Updated: August 01, 2013 at 15:52 |
PW121937 |
disease
Canavan DiseaseRattus norvegicus
Canavan Disease (Canavan-Van Bogaert-Bertrand Disease; Aminoacylase 2 Deficiency; Spongy Degeneration of the Central Nervous System; Aspartoacylase Deficiency; ASP Deficiency; ACY2 Deficiency; ASPA) is a rare autosomal recessive disease caused by a defect in the ASPA gene which codes for aspartoacylase. A deficiency in this enzyme results in accumulation of N-Acetyl-L-aspartic acid in plasma, spinal fluid, and urine. Symptoms, which present at birth, include myclonus, irritability, hypotonia, motor retardation, and poor head control. The neurological complications are due to demyelination of neurons and leukodystrophy. Premature death often results, though lithium citrate can be used as a treatment.
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Creator: Ana Marcu Created On: September 10, 2018 at 15:51 Last Updated: September 10, 2018 at 15:51 |
PW127346 |
disease
Canavan DiseaseHomo sapiens
Canavan Disease (Canavan-Van Bogaert-Bertrand Disease; Aminoacylase 2 Deficiency; Spongy Degeneration of the Central Nervous System; Aspartoacylase Deficiency; ASP Deficiency; ACY2 Deficiency; ASPA) is a rare autosomal recessive disease caused by a defect in the ASPA gene which codes for aspartoacylase. A deficiency in this enzyme results in accumulation of N-Acetyl-L-aspartic acid in plasma, spinal fluid, and urine. Symptoms, which present at birth, include myclonus, irritability, hypotonia, motor retardation, and poor head control. The neurological complications are due to demyelination of neurons and leukodystrophy. Premature death often results, though lithium citrate can be used as a treatment.
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Creator: Ray Kruger Created On: December 13, 2022 at 16:24 Last Updated: December 13, 2022 at 16:24 |
PW121712 |
disease
Canavan DiseaseMus musculus
Canavan Disease (Canavan-Van Bogaert-Bertrand Disease; Aminoacylase 2 Deficiency; Spongy Degeneration of the Central Nervous System; Aspartoacylase Deficiency; ASP Deficiency; ACY2 Deficiency; ASPA) is a rare autosomal recessive disease caused by a defect in the ASPA gene which codes for aspartoacylase. A deficiency in this enzyme results in accumulation of N-Acetyl-L-aspartic acid in plasma, spinal fluid, and urine. Symptoms, which present at birth, include myclonus, irritability, hypotonia, motor retardation, and poor head control. The neurological complications are due to demyelination of neurons and leukodystrophy. Premature death often results, though lithium citrate can be used as a treatment.
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Creator: Ana Marcu Created On: September 10, 2018 at 15:49 Last Updated: September 10, 2018 at 15:49 |
PW145882 |
drug action
Canagliflozin Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 16:53 Last Updated: October 07, 2023 at 16:53 |
PW176363 |
Camphor Predicted Metabolism PathwayHomo sapiens
Metabolites of Camphor are predicted with biotransformer.
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Creator: Omolola Created On: December 07, 2023 at 15:49 Last Updated: December 07, 2023 at 15:49 |
PW145498 |
drug action
Camphor Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 15:56 Last Updated: October 07, 2023 at 15:56 |
PW123600 |
signaling
cAMP signallingBos taurus
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Creator: Guest: Anonymous Created On: September 24, 2019 at 03:36 Last Updated: September 24, 2019 at 03:36 |
PW126957 |
Camellia nitidissima triterpenoid biosynthesis 1653525001Camellia nitidissima
Camellia nitidissima is common traditional ethnic medicine in Guangxi, which takes effect by clearing away heat and toxic materials and diuretic detumescence.
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Creator: WishartLab Created On: May 25, 2022 at 18:30 Last Updated: May 25, 2022 at 18:30 |