Biogenic amine synthesis

Pathway network for the Biogenic amine synthesis SuperPath

Sources:
  • WikiPathways
  • Reactome
  • PubChem

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Biogenic amine synthesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hyperphenylalaninemia, bh4-deficient, aEnrichmentGCH1, PAH, PTS, QDPR10.36
2Dystonia, dopa-responsiveEnrichmentGCH1, TH5.47
3Hyperphenylalaninemia, bh4-deficient, bEnrichmentGCH1, PTS5.47
4Hyperphenylalaninemia due to tetrahydrobiopterin deficiencyEnrichmentPTS, QDPR5.47
5DystoniaEnrichmentGCH1, SPR, TH5.15
6RasopathyEnrichmentDDC, PAH3.44
7Orthostatic hypotension 1EnrichmentDBH3.35
8Aromatic l-amino acid decarboxylase deficiencyEnrichmentDDC3.35
9Dopamine beta-hydroxylase deficiencyEnrichmentDBH3.35
10Segawa syndrome, autosomal recessiveEnrichmentTH3.23
11Parkinsonism-dystonia 1, infantile-onsetEnrichmentSLC6A33.18
12Classic dopamine transporter deficiency syndromeEnrichmentSLC6A33.18
13Catechol-o-methyltransferase activity, variation inEnrichmentCOMT3.18
14Parkinsonism-dystonia, infantileEnrichmentSLC6A33.18
15Apnea, central sleepEnrichmentCHAT2.96
16Yt blood group antigenEnrichmentACHE2.96
17Developmental and epileptic encephalopathy 89EnrichmentGAD12.96
18Brunner syndromeEnrichmentMAOA2.96
19Aspiration pneumoniaEnrichmentCHAT2.96
20Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuriaEnrichmentPAH2.96
21Hyperphenylalaninemia, mild, non-bh4-deficientEnrichmentDNAJC122.96
22Megaloblastic anemia due to dihydrofolate reductase deficiencyEnrichmentDHFR2.96
23Hyperphenylalaninemia due to dnajc12 deficiencyEnrichmentDNAJC122.96
24Major affective disorder 1EnrichmentTPH22.88
25Parkinsonism-dystonia 2, infantile-onsetEnrichmentSLC18A22.88
26Gilles de la tourette syndromeEnrichmentHDC2.66
27Neurodevelopmental disorder with spasticity, hypomyelinating leukodystrophy, and brain abnormalitiesEnrichmentPAH2.66
28Myasthenic syndrome, congenital, 21, presynapticEnrichmentCHAT2.66
29Hyperphenylalaninemia, bh4-deficient, cEnrichmentQDPR2.66
30Dystonia, dopa-responsive, due to sepiapterin reductase deficiencyEnrichmentSPR2.66
31Tobacco addictionEnrichmentSLC6A32.58
32Major depressive disorderEnrichmentTPH22.48
33Myasthenic syndrome, congenital, 6, presynapticEnrichmentCHAT2.48
34Pituitary hormone deficiency, combined, 2EnrichmentPAH2.48
35Bronchopulmonary dysplasiaEnrichmentCHAT2.48
36Familial adenomatous polyposis 4EnrichmentDHFR2.48
37Gtp cyclohydrolase 1-deficient dopa-responsive dystoniaEnrichmentGCH12.48
38PhenylketonuriaEnrichmentPAH2.35
39Propionic acidemiaEnrichmentPAH2.35
40Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalitiesEnrichmentGAD12.35
41Spastic quadriplegic cerebral palsyEnrichmentGAD12.35
42Sleep disorderEnrichmentGCH12.26
43Digeorge syndromeEnrichmentCOMT2.10
44Gastroesophageal refluxEnrichmentCHAT2.05
45Myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiencyEnrichmentCHAT1.96
46Presynaptic congenital myasthenic syndromesEnrichmentCHAT1.92
47Lactic acidosisEnrichmentCHAT1.88
48Pulmonary hypertension, primary, 1EnrichmentPAH1.85
49Congenital myasthenic syndromeEnrichmentCHAT1.81
50Endometrial cancerEnrichmentDHFR1.64
51Bardet-biedl syndromeEnrichmentCOMT1.56
52SchizophreniaEnrichmentCOMT1.41
53Breast cancerEnrichmentPAH1.10
54Inherited cancer-predisposing syndromeEnrichmentDHFR0.86

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