Hormone ligand-binding receptors

No Pathway Network information available for Hormone ligand-binding receptors

Pathways in the Hormone ligand-binding receptors SuperPath

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

Disorders associated with Hormone ligand-binding receptors SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Normosmic congenital hypogonadotropic hypogonadismEnrichmentGNRH1, GNRHR3.96
2Hypogonadotropic hypogonadism 23 with or without anosmiaEnrichmentLHB3.05
3Ovarian dysgenesis 1EnrichmentFSHR3.05
4Twinning, dizygoticEnrichmentFSHR3.05
5Hypothyroidism, congenital, nongoitrous, 4EnrichmentTSHB3.05
6Ovarian hyperstimulation syndromeEnrichmentFSHR3.05
7Hypogonadotropic hypogonadism 12 with or without anosmiaEnrichmentGNRH13.05
8AmenorrheaEnrichmentFSHR3.05
9Isolated gonadotropin-releasing hormone deficiencyEnrichmentGNRHR3.05
10Precocious puberty, male-limitedEnrichmentLHCGR2.75
11Leydig cell hypoplasia, type iEnrichmentLHCGR2.75
12Hypogonadotropic hypogonadism 24 with or without anosmiaEnrichmentFSHB2.75
13Hyperthyroidism, familial gestationalEnrichmentTSHR2.75
14Leydig cell hypoplasia type iiEnrichmentLHCGR2.75
15Hyperthyroidism, nonautoimmuneEnrichmentTSHR2.58
16Hypothyroidism, congenital, nongoitrous, 1EnrichmentTSHR2.58
17Gonadal dysgenesisEnrichmentFSHR2.58
18Familial hyperthyroidism due to mutations in tsh receptorEnrichmentTSHR2.58
19Smith-lemli-opitz syndromeEnrichmentTSHR2.45
20PseudohermaphroditismEnrichmentLHCGR2.35
21InfertilityEnrichmentGNRHR2.28
22Hypothyroidism, congenital, nongoitrous, 2EnrichmentTSHR2.21
23Hypogonadotropic hypogonadismEnrichmentGNRHR2.10
24Congenital hypothyroidismEnrichmentTSHR1.98
2546 xx gonadal dysgenesisEnrichmentFSHR1.98
26Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentGNRHR1.91
27Perrault syndrome 1EnrichmentFSHR1.85
28EpilepsyEnrichmentTSHR1.46
29Ovarian cancerEnrichmentTSHR1.07

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