Cell differentiation - expanded index

No Pathway Network information available for Cell differentiation - expanded index

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

Disorders associated with Cell differentiation - expanded index SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Precursor t-cell acute lymphoblastic leukemiaEnrichmentTLX1, TLX33.25
2T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.81
3Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.81
4Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.81
5Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.81
6Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.37
7Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.37
8Congenital myopathy 19EnrichmentPAX72.37
9Congenital myopathy 17EnrichmentMYOD12.37
105q14.3 microdeletion syndromeEnrichmentMEF2C2.37
11Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.37
12Mef2c-related disorderEnrichmentMEF2C2.37
13Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.33
14Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT32.33
15Hyper ige syndromeEnrichmentSTAT32.33
16Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactylyEnrichmentRUNX22.07
17Permanent neonatal diabetes mellitusEnrichmentSTAT31.91
18Cleidocranial dysplasia 1EnrichmentRUNX21.89
19Weaver syndromeEnrichmentEZH21.89
20Cleidocranial dysplasiaEnrichmentRUNX21.89
21Microphthalmia, syndromic 3EnrichmentSOX21.77
22Acute promyelocytic leukemiaEnrichmentSTAT31.70
23Rhabdomyosarcoma 2EnrichmentPAX71.67
24Myopathy, centronuclear, 1EnrichmentMYOD11.60
25Diffuse large b-cell lymphomaEnrichmentSTAT31.54
26Visceral heterotaxyEnrichmentLEFTY21.47
27NanophthalmosEnrichmentSOX21.34
28Septooptic dysplasiaEnrichmentSOX21.30
29Macs syndromeEnrichmentSOX21.09
30MicrophthalmiaEnrichmentSOX21.05
31Fetal akinesia deformation sequence 1EnrichmentMYOD10.83
32Distal arthrogryposisEnrichmentMYOD10.78
33Nephrotic syndromeEnrichmentRUNX20.77
34Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.66
35Autism spectrum disorderEnrichmentMEF2C0.43
36Inherited cancer-predisposing syndromeEnrichmentEZH20.36

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