Autosomal recessive osteopetrosis pathways

No Pathway Network information available for Autosomal recessive osteopetrosis pathways

Pathways in the Autosomal recessive osteopetrosis pathways SuperPath

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

Disorders associated with Autosomal recessive osteopetrosis pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1OsteopetrosisEnrichmentCLCN7, OSTM1, SNX10, TCIRG110.81
2Autosomal recessive osteopetrosisEnrichmentCLCN7, SNX10, TCIRG1, TNFSF1110.77
3Osteopetrosis, autosomal recessive 6EnrichmentCLCN7, PLEKHM1, TCIRG19.39
4DysosteosclerosisEnrichmentTCIRG1, TNFRSF11A5.75
5Osteopetrosis, autosomal dominant 2EnrichmentCLCN73.09
6Osteopetrosis, autosomal recessive 7EnrichmentTNFRSF11A3.09
7Immunodeficiency 15bEnrichmentIKBKB3.09
8Immunodeficiency 15aEnrichmentIKBKB3.09
9Hypopigmentation, organomegaly, and delayed myelination and developmentEnrichmentCLCN73.09
10Charcot-marie-tooth disease, axonal, type 2bEnrichmentRAB7A3.09
11Charcot-marie-tooth disease type 2bEnrichmentRAB7A3.09
12Osteopetrosis, autosomal dominant 3EnrichmentPLEKHM13.09
13Osteopetrosis, autosomal recessive 8EnrichmentSNX103.09
14Familial expansile osteolysisEnrichmentTNFRSF11A2.79
15Paget disease of bone 5, juvenile-onsetEnrichmentTNFRSF11A2.79
16Osteopetrosis, autosomal recessive 4EnrichmentCLCN72.79
17Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.79
18Osteopetrosis, autosomal recessive 2EnrichmentTNFSF112.79
19Osteopetrosis, autosomal recessive 5EnrichmentOSTM12.79
20Osteopetrosis, autosomal recessive 1EnrichmentTCIRG12.79
21OsteosclerosisEnrichmentCLCN72.79
22Common variable immunodeficiency 12EnrichmentNFKB12.79
23Infantile osteopetrosis with neuroaxonal dysplasiaEnrichmentOSTM12.79
24ChoreoacanthocytosisEnrichmentTCIRG12.61
25Neutropenia, severe congenital, 1, autosomal dominantEnrichmentTCIRG12.61
26Adult-onset myasthenia gravisEnrichmentTNFRSF11A2.61
27Paget disease of bone 2, early-onsetEnrichmentTNFRSF11A2.49
28Paget's disease of bone 2EnrichmentTNFRSF11A2.49
29Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.39
30Autosomal dominant severe congenital neutropeniaEnrichmentTCIRG12.39
31Common variable immunodeficiencyEnrichmentNFKB12.25
32Severe congenital neutropeniaEnrichmentTCIRG12.19
33Ciliary dyskinesia, primary, 3EnrichmentNFKB12.09
34Severe combined immunodeficiencyEnrichmentIKBKB1.58

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