Growth hormone receptor signaling

No Pathway Network information available for Growth hormone receptor signaling

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

Disorders associated with Growth hormone receptor signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK2, STAT35.05
2Primary ovarian insufficiencyEnrichmentJAK2, PRLR, SH2B14.47
3Type 2 diabetes mellitusEnrichmentIRS1, IRS2, PTPN14.27
4Specific learning disabilityEnrichmentGHR, PTPN114.20
5Acute promyelocytic leukemiaEnrichmentSTAT3, STAT5B3.64
6Diffuse large b-cell lymphomaEnrichmentSOCS1, STAT33.30
7MetachondromatosisEnrichmentPTPN112.96
8Leopard syndrome 1EnrichmentPTPN112.96
9Multiple fibroadenomas of the breastEnrichmentPRLR2.96
10Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B2.96
11Laron syndromeEnrichmentGHR2.96
12HyperprolactinemiaEnrichmentPRLR2.96
13Growth hormone insensitivity, partialEnrichmentGHR2.96
14Familial hyperprolactinemiaEnrichmentPRLR2.96
15Severe early-onset obesity-insulin resistance syndrome due to sh2b1 deficiencyEnrichmentSH2B12.96
16Malignant astrocytomaEnrichmentPTPN112.96
17Dermatitis, atopic, 4EnrichmentSOCS32.75
18Noonan syndrome 13EnrichmentMAPK12.75
19T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.75
20Immunodeficiency 31aEnrichmentSTAT12.75
21Immunodeficiency 31bEnrichmentSTAT12.75
22Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.75
23Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.75
24Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.75
25Vegetative pyoderma gangrenosumEnrichmentPTPN62.75
26Bullous pyoderma gangrenosumEnrichmentPTPN62.75
27Pustular pyoderma gangrenosumEnrichmentPTPN62.75
28Classic pyoderma gangrenosumEnrichmentPTPN62.75
29Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.75
30Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.66
31Chromosome 16p11.2 deletion syndrome, 220-kbEnrichmentSH2B12.66
32Growth hormone deficiency, isolated partialEnrichmentGHR2.66
33Thrombocythemia 3EnrichmentJAK22.66
34Werner syndromeEnrichmentPTPN112.66
35Kowarski syndromeEnrichmentGH12.66
36Chromosome 16p11.2 deletion syndrome, 593-kbEnrichmentSH2B12.66
37PolycythemiaEnrichmentJAK22.66
38Short stature due to growth hormone qualitative anomalyEnrichmentGH12.66
39Hypereosinophilic syndromeEnrichmentJAK22.66
40Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.66
41Polycythemia veraEnrichmentJAK22.48
42Isolated growth hormone deficiency, type ibEnrichmentGH12.48
43Tricuspid valve insufficiencyEnrichmentPTPN112.48
44Immunodeficiency 31cEnrichmentSTAT12.45
45Inflammatory skin and bowel disease, neonatal, 1EnrichmentADAM172.45
46Isolated growth hormone deficiency, type iiEnrichmentGH12.35
47Erythrocytosis, familial, 1EnrichmentJAK22.35
48Budd-chiari syndromeEnrichmentJAK22.35
49Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.35
50Noonan syndrome with multiple lentiginesEnrichmentPTPN112.35
51Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.28
52Immune thrombocytopeniaEnrichmentSOCS12.28
53Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.28
54Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS12.28
55Bacteremia 2EnrichmentCISH2.28
56Hyper ige syndromeEnrichmentSTAT32.28
57Neonatal inflammatory skin and bowel diseaseEnrichmentADAM172.28
58LymphomaEnrichmentPTPN112.26
59Myeloproliferative neoplasmEnrichmentJAK22.26
60Patent ductus arteriosusEnrichmentPTPN112.18
61Anemia, autoimmune hemolyticEnrichmentSOCS12.15
62Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.15
63TuberculosisEnrichmentCISH2.15
64MyelofibrosisEnrichmentJAK22.11
65Noonan syndrome 3EnrichmentPTPN112.11
66Essential thrombocythemiaEnrichmentJAK22.11
67Isolated growth hormone deficiency, type iaEnrichmentGH12.05
68Isolated split hand-split foot malformationEnrichmentBTRC2.05
69Leukemia, acute lymphoblastic 3EnrichmentJAK22.00
70Chronic mucocutaneous candidiasisEnrichmentSTAT11.98
71Pectus excavatumEnrichmentPTPN111.92
72EpicanthusEnrichmentPTPN111.88
73Juvenile myelomonocytic leukemiaEnrichmentPTPN111.88
74Congenital long qt syndromeEnrichmentPTPN111.88
75Permanent neonatal diabetes mellitusEnrichmentSTAT31.85
76Hypercholesterolemia, familial, 1EnrichmentGHR1.85
77Familial hypercholesterolemiaEnrichmentGHR1.78
78Noonan syndrome and noonan-related syndromeEnrichmentPTPN111.78
79Patent foramen ovaleEnrichmentPTPN111.70
80Noonan syndrome 1EnrichmentPTPN111.60
81ScoliosisEnrichmentPTPN111.58
82Hydrops fetalis, nonimmuneEnrichmentPTPN111.55
83RasopathyEnrichmentPTPN111.55
84StrabismusEnrichmentPTPN111.53
85Heart, malformation ofEnrichmentMAPK11.50
86Long qt syndrome 1EnrichmentPTPN111.49
87Non-immune hydrops fetalisEnrichmentPTPN111.47
88MalariaEnrichmentCISH1.40
89Leukemia, acute myeloidEnrichmentJAK21.36
90Hypertrophic cardiomyopathyEnrichmentPTPN111.33
91ThrombocytopeniaEnrichmentPTPN111.29
92Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.22
93Systemic lupus erythematosusEnrichmentSOCS11.18
94Autism spectrum disorderEnrichmentPTPN110.94
95MicrocephalyEnrichmentPTPN110.89
96Inherited cancer-predisposing syndromeEnrichmentPTPN110.86

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