Involvement of -secretase in neurodegenerative diseases

No Pathway Network information available for Involvement of -secretase in neurodegenerative diseases

Pathways in the Involvement of -secretase in neurodegenerative diseases SuperPath

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

Disorders associated with Involvement of -secretase in neurodegenerative diseases SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Alzheimer's diseaseEnrichmentAPP, MAPT4.00
2Alzheimer disease, familial, 1EnrichmentAPP, MAPT3.76
3Parkinson disease, late-onsetEnrichmentMAPT, SNCA3.45
4Proteus syndromeEnrichmentAKT12.93
5Parkinson disease 1, autosomal dominantEnrichmentSNCA2.93
6Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.93
7Parkinson disease 4, autosomal dominantEnrichmentSNCA2.93
8Developmental and epileptic encephalopathy 58EnrichmentNTRK22.93
9Parkinson-dementia syndromeEnrichmentMAPT2.93
10Supranuclear palsy, progressive, 1EnrichmentMAPT2.93
11Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.93
12Progressive supranuclear palsyEnrichmentMAPT2.93
13Cerebral amyloid angiopathy, app-relatedEnrichmentAPP2.93
14Immunodeficiency 31aEnrichmentSTAT12.93
15Cowden syndrome 6EnrichmentAKT12.93
16Immunodeficiency 31bEnrichmentSTAT12.93
17Obesity, hyperphagia, and developmental delayEnrichmentNTRK22.93
18Classic progressive supranuclear palsy syndromeEnrichmentMAPT2.93
19Atypical progressive supranuclear palsy syndromeEnrichmentMAPT2.93
20Capillary hemangiomaEnrichmentAKT32.93
21Tardbp-related predominantly upper-limb distal myopathyEnrichmentTARDBP2.93
22Akt2-related familial partial lipodystrophyEnrichmentAKT22.93
23Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMAPT, TARDBP2.68
24Cerebral amyloid angiopathy, cst3-relatedEnrichmentAPP2.63
25Pick disease of brainEnrichmentMAPT2.63
26Immunodeficiency 31cEnrichmentSTAT12.63
27Parkinson disease 15, autosomal recessive early-onsetEnrichmentSNCA2.63
28Senior-loken syndrome 7EnrichmentAKT32.63
29Bardet-biedl syndrome 16EnrichmentAKT32.63
30Intellectual developmental disorder, autosomal dominant 58EnrichmentSET2.63
31Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT32.33
32Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT32.33
33Dementia, lewy bodyEnrichmentSNCA2.23
34Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentTARDBP2.23
35HemimegalencephalyEnrichmentAKT32.23
36DementiaEnrichmentMAPT2.23
37Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndromeEnrichmentBDNF2.15
38Chronic mucocutaneous candidiasisEnrichmentSTAT12.15
39Breast adenocarcinomaEnrichmentAKT12.15
40Semantic dementiaEnrichmentMAPT2.08
41Alzheimer's disease 1EnrichmentAPP2.08
42Motor neuron diseaseEnrichmentTARDBP2.08
43Pilomyxoid astrocytomaEnrichmentNTRK22.08
44MegacolonEnrichmentAKT32.08
45Early-onset autosomal dominant alzheimer diseaseEnrichmentAPP2.08
46Congenital central hypoventilation syndromeEnrichmentBDNF1.98
47Progressive non-fluent aphasiaEnrichmentMAPT1.98
48Cowden syndromeEnrichmentAKT11.98
49Behavioral variant of frontotemporal dementiaEnrichmentMAPT1.98
50Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTARDBP1.93
51PolymicrogyriaEnrichmentAKT31.93
52Frontotemporal dementia 1EnrichmentMAPT1.89
53Early-onset parkinson's diseaseEnrichmentSNCA1.85
54MeningiomaEnrichmentAKT11.85
55Precursor t-cell acute lymphoblastic leukemiaEnrichmentSET1.57
56Type 2 diabetes mellitusEnrichmentAKT21.31
57West syndromeEnrichmentNTRK21.30
58Hereditary breast carcinomaEnrichmentAKT11.30
59Body mass index quantitative trait locus 11EnrichmentBDNF1.24
60Autosomal dominant non-syndromic intellectual disabilityEnrichmentSET1.24
61Undetermined early-onset epileptic encephalopathyEnrichmentNTRK21.19
62Breast cancerEnrichmentAKT11.07
63Colorectal cancerEnrichmentAKT11.01
64Ovarian cancerEnrichmentAKT10.95

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