NAD metabolism

Pathway network for the NAD metabolism SuperPath

Sources:
  • GeneGo (Thomson Reuters)
  • WikiPathways
  • PubChem

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

Disorders associated with NAD metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Congenital nad deficiency disorderEnrichmentHAAO, KYNU, NADSYN16.60
2Glucocorticoid deficiency 4 with or without mineralocorticoid deficiencyEnrichmentNNT3.83
3Spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosisEnrichmentNMNAT13.66
4Leber congenital amaurosis 9EnrichmentNMNAT13.35
5Familial glucocorticoid deficiencyEnrichmentNNT3.13
6Calcification of joints and arteriesEnrichmentNT5E2.93
7Lethal brain and heart developmental defectsEnrichmentSIRT62.93
8DiarrheaEnrichmentNMNAT12.88
9HypertryptophanemiaEnrichmentTDO22.79
10Vertebral, cardiac, renal, and limb defects syndrome 3EnrichmentNADSYN12.79
11Renu syndromeEnrichmentSIRT42.45
12Anemia, congenital, nonspherocytic hemolytic, 8EnrichmentNT5C3A2.39
13Hypophosphatasia, adultEnrichmentALPL2.39
14Blood group, dombrock systemEnrichmentART42.39
15HydroxykynureninuriaEnrichmentKYNU2.39
16Hypophosphatasia, childhoodEnrichmentALPL2.39
17Arterial calcification, generalized, of infancy, 1EnrichmentENPP12.39
18Vertebral, cardiac, renal, and limb defects syndrome 2EnrichmentKYNU2.39
19Ossification of the posterior longitudinal ligament of spineEnrichmentENPP12.39
20Drug metabolism, poor, cyp2d6-relatedEnrichmentCYP2D62.39
21Hypophosphatemic rickets, autosomal recessive, 2EnrichmentENPP12.39
22Cole diseaseEnrichmentENPP12.39
23Purine nucleoside phosphorylase deficiencyEnrichmentPNP2.39
24Prenatal benign hypophosphatasiaEnrichmentALPL2.39
25Hypopigmentation-punctate palmoplantar keratoderma syndromeEnrichmentENPP12.39
26Alpi-related inflammatory bowel diseaseEnrichmentALPI2.39
27Cone dystrophyEnrichmentNMNAT12.28
28Methemoglobinemia due to deficiency of methemoglobin reductaseEnrichmentCYB5R32.09
29Alpha-thalassemia/impaired intellectual development syndrome, x-linkedEnrichmentALPL2.09
30Vertebral, cardiac, renal, and limb defects syndrome 1EnrichmentHAAO2.09
31Autosomal recessive hypophosphatemic ricketsEnrichmentENPP12.09
32Catel-manzke syndromeEnrichmentKYNU2.09
33Spastic paraplegia 45, autosomal recessiveEnrichmentNT5C22.09
34HypophosphatasiaEnrichmentALPL2.09
35Alpha thalassemia-x-linked intellectual disability syndromeEnrichmentALPL2.09
36Dystonia 28, childhood-onsetEnrichmentENPP12.09
37Arterial calcification of infancyEnrichmentENPP12.09
38Hereditary methemoglobinemiaEnrichmentCYB5R32.09
39Hypophosphatasia, infantileEnrichmentALPL1.92
40Cone-rod dystrophy 2EnrichmentNMNAT11.82
41Congenital myopathy 1a, autosomal dominant, with malignant hyperthermiaEnrichmentCYB5R31.79
42Congenital myopathy 1aEnrichmentCYB5R31.79
43Leber plus diseaseEnrichmentNMNAT11.68
44Pseudoxanthoma elasticumEnrichmentENPP11.62
45Hypophosphatemic ricketsEnrichmentENPP11.55
46Hereditary retinal dystrophyEnrichmentNMNAT11.20
47Fundus dystrophyEnrichmentNMNAT11.20
48Primary ovarian insufficiencyEnrichmentSIRT61.17
49Brittle bone disorderEnrichmentALPL1.05
50Severe combined immunodeficiencyEnrichmentPNP0.90
51Type 2 diabetes mellitusEnrichmentENPP10.80
52Body mass index quantitative trait locus 11EnrichmentENPP10.73

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