GPCRs, other

No Pathway Network information available for GPCRs, other

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

Disorders associated with GPCRs, other SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hypogonadotropic hypogonadismEnrichmentGNRHR, PROKR22.74
2Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentGNRHR, PROKR22.35
3Vibratory urticariaEnrichmentADGRE22.14
4Hypogonadotropic hypogonadism 3 with or without anosmiaEnrichmentPROKR22.14
5Nystagmus 6, congenital, x-linkedEnrichmentGPR1432.14
6Curry-jones syndromeEnrichmentSMO2.14
7Cortical dysplasia, complex, with other brain malformations 14aEnrichmentADGRG12.14
8White blood cell count quantitative trait locus 1EnrichmentACKR12.14
9Mandibulofacial dysostosis with alopeciaEnrichmentEDNRA2.14
10Tremor, hereditary essential, 1EnrichmentDRD32.14
11Ovarian dysgenesis 1EnrichmentFSHR2.14
12Spinocerebellar ataxia, autosomal recessive 13EnrichmentGRM12.14
13Twinning, dizygoticEnrichmentFSHR2.14
14Febrile seizures, familial, 4EnrichmentADGRV12.14
15Congenital disorder of glycosylation, type icEnrichmentALG62.14
16Ovarian hyperstimulation syndromeEnrichmentFSHR2.14
17AmenorrheaEnrichmentFSHR2.14
18Cortical dysplasia, complex, with other brain malformations 14bEnrichmentADGRG12.14
19Type 1 diabetes mellitus 22EnrichmentCCR52.14
20Chorea, childhood-onset, with psychomotor retardationEnrichmentGPR882.14
21Celsr1-related late-onset primary lymphedemaEnrichmentCELSR12.14
22Spinocerebellar ataxia 44EnrichmentGRM12.14
23Isolated growth hormone deficiency, type ivEnrichmentGHRHR2.14
24Whim syndrome 2EnrichmentCXCR22.14
25Isolated gonadotropin-releasing hormone deficiencyEnrichmentGNRHR2.14
26Autonomic nervous system diseaseEnrichmentDRD42.14
27Acute encephalopathy with biphasic seizures and late reduced diffusionEnrichmentADORA2A2.14
28Autosomal recessive severe congenital neutropenia due to cxcr2 deficiencyEnrichmentCXCR22.14
29Chondromyxoid fibromaEnrichmentGRM12.14
30Human immunodeficiency virus type 1EnrichmentCCR5, CXCR12.13
31Normosmic congenital hypogonadotropic hypogonadismEnrichmentGNRHR, PROKR22.13
32Pallister-hall-like syndromeEnrichmentSMO1.84
33West nile virusEnrichmentCCR51.84
34Usher syndrome, type iicEnrichmentADGRV11.84
35Obsessive-compulsive disorderEnrichmentHTR2A1.84
36Lymphatic malformation 9EnrichmentCELSR11.84
37Prune belly syndromeEnrichmentCHRM31.67
38Hypogonadotropic hypogonadism 2 with or without anosmiaEnrichmentPROKR21.67
39Hepatitis c virusEnrichmentCCR51.67
40Isolated growth hormone deficiency, type ibEnrichmentGHRHR1.67
41Gonadal dysgenesisEnrichmentFSHR1.67
42Orofaciodigital syndrome iiiEnrichmentCELSR21.54
43Hypogonadotropic hypogonadism 1 with or without anosmiaEnrichmentPROKR21.45
44Major depressive disorderEnrichmentHTR2A1.45
45Albinism, ocular, type iEnrichmentGPR1431.37
46Congenital anomalies of kidney and urinary tract 1EnrichmentCELSR31.37
47AlbinismEnrichmentGPR1431.37
48InfertilityEnrichmentGNRHR1.37
49Usher syndrome, type iiaEnrichmentADGRV11.31
50Narcolepsy 1EnrichmentP2RY111.25
51Essential tremorEnrichmentDRD31.25
52Tracheoesophageal fistula with or without esophageal atresiaEnrichmentCELSR21.20
53Bilateral perisylvian polymicrogyriaEnrichmentADGRG11.20
54SchizophreniaEnrichmentDRD3, HTR2A1.17
55Isolated tracheo-esophageal fistulaEnrichmentCELSR21.16
56Epilepsy, idiopathic generalizedEnrichmentADGRV11.12
57Usher syndrome type 2EnrichmentADGRV11.12
58Septooptic dysplasiaEnrichmentPROKR21.08
59MeningiomaEnrichmentSMO1.08
6046 xx gonadal dysgenesisEnrichmentFSHR1.08
61Neural tube defectsEnrichmentCELSR11.05
62Generalized epilepsy with febrile seizures plusEnrichmentADGRV11.02
63Pituitary stalk interruption syndromeEnrichmentPROKR21.02
64Usher syndrome, type iEnrichmentADGRV10.99
65Male infertility with spermatogenesis disorderEnrichmentPROKR20.99
66Perrault syndrome 1EnrichmentFSHR0.96
67Esophageal atresia/tracheoesophageal fistulaEnrichmentCELSR20.89
68Attention deficit-hyperactivity disorderEnrichmentDRD40.83
69MalariaEnrichmentACKR10.81
70Kallmann syndromeEnrichmentPROKR20.81
71Ear malformationEnrichmentADGRV10.80
72StrabismusEnrichmentADGRG10.75
73Hirschsprung disease 1EnrichmentSMO0.72
74Cystic fibrosisEnrichmentEDNRA0.68
75Usher syndromeEnrichmentADGRV10.67
76Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPROKR20.48
77Deafness, autosomal recessiveEnrichmentADGRV10.43
78Autosomal recessive nonsyndromic deafnessEnrichmentADGRV10.43
79Rare genetic deafnessEnrichmentADGRV10.36
80Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentADGRV10.32
81Congenital nervous system abnormalityEnrichmentADGRG10.27
82Nervous system diseaseEnrichmentADGRG10.27
83Retinitis pigmentosaEnrichmentADGRV10.10
84Hereditary retinal dystrophyEnrichmentADGRV10.06
85Fundus dystrophyEnrichmentADGRV10.06

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