Innate Lymphoid Cells Differentiation

No Pathway Network information available for Innate Lymphoid Cells Differentiation

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

Disorders associated with Innate Lymphoid Cells Differentiation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Immunodeficiency 104, severe combinedEnrichmentIL7R, PTPRC4.46
2Systemic lupus erythematosusEnrichmentETS1, IL10, ITGAM, TNF4.10
3Psoriatic arthritisEnrichmentLTA, TNF3.99
4Human immunodeficiency virus type 1EnrichmentCCL3, IFNG, IL103.82
5Behcet syndromeEnrichmentIL10, IL12A, IL23R3.75
6Acute myeloid leukemia with t(8;21)(q22;q22) translocationEnrichmentKIT, RUNX13.47
7Oligoarticular juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.15
8Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.15
9Rheumatoid arthritisEnrichmentCD244, IL102.92
10Primary biliary cholangitisEnrichmentIL12A, IL12RB12.92
11AsthmaEnrichmentIL13, TNF2.74
12Type 1 diabetes mellitus 10EnrichmentIL2RA2.23
13Systemic lupus erythematosus 6EnrichmentITGAM2.23
14Leprosy 4EnrichmentLTA2.23
15Skin/hair/eye pigmentation, variation in, 8EnrichmentIRF42.23
16Mastocytosis, cutaneousEnrichmentKIT2.23
17Immunodeficiency 30EnrichmentIL12RB12.23
18Hajdu-cheney syndromeEnrichmentNOTCH22.23
19Alagille syndrome 2EnrichmentNOTCH22.23
20Skeletal defects, genital hypoplasia, and impaired intellectual developmentEnrichmentZBTB162.23
21Spinocerebellar ataxia, autosomal recessive 7EnrichmentTPP12.23
22Immunodeficiency 116EnrichmentCD8A2.23
23Retinitis pigmentosa 85EnrichmentAHR2.23
24Immunodeficiency 69EnrichmentIFNG2.23
25Agammaglobulinemia 10, autosomal dominantEnrichmentSPI12.23
26Immunodeficiency 130 with hpv-related verrucosisEnrichmentIL72.23
27Immunodeficiency 131EnrichmentIRF42.23
28Immunodeficiency 63 with lymphoproliferation and autoimmunityEnrichmentIL2RB2.23
29Okt4 epitope deficiencyEnrichmentCD42.23
30Graft-versus-host diseaseEnrichmentIL102.23
31Foveal hypoplasia 3EnrichmentAHR2.23
32Intellectual developmental disorder with paroxysmal dyskinesia or seizuresEnrichmentPDE2A2.23
33Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.23
34Allergic rhinitisEnrichmentIL132.23
35Immunodeficiency 42EnrichmentRORC2.23
36Psoriasis 7EnrichmentIL23R2.23
37Inflammatory bowel disease 17EnrichmentIL23R2.23
38Immunodeficiency 105, severe combinedEnrichmentPTPRC2.23
39Immunodeficiency, common variable, 13EnrichmentIKZF12.23
40Immunodeficiency 79EnrichmentCD42.23
41Cd45 deficiencyEnrichmentPTPRC2.23
42Immunodeficiency 88EnrichmentTBX212.23
43Chronic mast cell leukemiaEnrichmentKIT2.23
44Combined immunodeficiency due to dimerization defective ikaros mutationEnrichmentIKZF12.23
45AgammaglobulinemiaEnrichmentSPI12.23
46Isolated bone marrow mastocytosisEnrichmentKIT2.23
47Smoldering systemic mastocytosisEnrichmentKIT2.23
48MastocytosisEnrichmentKIT2.23
49Early-onset combined immunodeficiency with low ig due to dominant negative ikaros mutationEnrichmentIKZF12.23
50Whipple diseaseEnrichmentIRF42.23
51Cutaneous mastocytomaEnrichmentKIT2.23
52Typical urticaria pigmentosaEnrichmentKIT2.23
53T-b+ severe combined immunodeficiency due to il-7ralpha deficiencyEnrichmentIL7R2.23
54Nodular urticaria pigmentosaEnrichmentKIT2.23
55Pseudoxanthomatous diffuse cutaneous mastocytosisEnrichmentKIT2.23
56Telangiectasia macularis eruptiva perstansEnrichmentKIT2.23
57Acute mast cell leukemiaEnrichmentKIT2.23
58Plaque-form urticaria pigmentosaEnrichmentKIT2.23
59Microcephaly-polymicrogyria-corpus callosum agenesis syndromeEnrichmentEOMES2.23
60Bullous diffuse cutaneous mastocytosisEnrichmentKIT2.23
61Testis seminomaEnrichmentKIT2.23
62Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndromeEnrichmentGATA31.93
63Storage pool platelet diseaseEnrichmentRUNX11.93
64Ceroid lipofuscinosis, neuronal, 2EnrichmentTPP11.93
65Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA1.93
66Piebald traitEnrichmentKIT1.93
67Ceroid lipofuscinosis, neuronal, 3EnrichmentTPP11.93
68Diamond-blackfan anemia-likeEnrichmentIKZF11.93
69Immunodeficiency 127EnrichmentTNF1.93
70Stevens-johnson syndromeEnrichmentIKZF11.93
71Multiple sclerosis 3EnrichmentIL7R1.93
72B-lymphoblastic leukemia/lymphoma with hyperdiploidyEnrichmentGATA31.93
73Hypoparathyroidism-deafness-renal disease syndromeEnrichmentGATA31.93
74Autosomal dominant nonsyndromic deafnessEnrichmentGATA31.93
75B-lymphoblastic leukemia/lymphoma with tEnrichmentKIT1.93
76Tafro syndromeEnrichmentRUNX11.93
77Severe combined immunodeficiencyEnrichmentIL7R, PTPRC1.79
78Jacobsen syndromeEnrichmentETS11.75
79Asthma, nasal polyps, and aspirin intoleranceEnrichmentTBX211.75
80Tuberous sclerosis 1EnrichmentIFNG1.75
81Platelet disorder, familial, with associated myeloid malignancyEnrichmentRUNX11.75
82Hepatitis c virusEnrichmentIFNG1.75
83Tuberous sclerosis 2EnrichmentIFNG1.75
84Testicular germ cell cancerEnrichmentKIT1.75
85Migraine without auraEnrichmentTNF1.75
86End stage renal diseaseEnrichmentGATA31.75
87Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with runx1EnrichmentRUNX11.75
88KeratoacanthomaEnrichmentNOTCH21.75
89Leukemia, acute myeloidEnrichmentKIT, RUNX11.63
90Immunodeficiency, common variable, 1EnrichmentICOS1.63
91Retinitis pigmentosa 26EnrichmentITGA41.63
92Blood platelet diseaseEnrichmentRUNX11.63
93Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)EnrichmentKIT1.63
94Cerebral malariaEnrichmentTNF1.63
95Inherited epidermodysplasia verruciformisEnrichmentIL71.63
96Systemic mastocytosis with associated hematologic neoplasmEnrichmentKIT1.63
97Hydatidiform mole, recurrent, 1EnrichmentNCR11.54
98Convulsions, familial infantile, with paroxysmal choreoathetosisEnrichmentPDE2A1.54
99Acute myeloid leukemia with maturationEnrichmentKIT1.54
100Vascular dementiaEnrichmentTNF1.54
101Aggressive systemic mastocytosisEnrichmentRUNX11.54
102Diffuse cutaneous systemic sclerosisEnrichmentCCR61.54
103Idiopathic aplastic anemiaEnrichmentIFNG1.54
104Angelman syndromeEnrichmentTPP11.46
105Testicular germ cell tumorEnrichmentKIT1.46
106PancytopeniaEnrichmentRUNX11.46
107Limited sclerodermaEnrichmentCCR61.46
108Il10-related early-onset inflammatory bowel diseaseEnrichmentIL101.46
109Gastrointestinal stromal tumorEnrichmentKIT1.39
110Leukemia, chronic myeloidEnrichmentRUNX11.39
111Paroxysmal dystoniaEnrichmentPDE2A1.39
112B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentIKZF11.39
113Choreatic diseaseEnrichmentPDE2A1.34
114Atypical chronic myeloid leukemia, bcr-abl1 negativeEnrichmentRUNX11.29
115Omenn syndromeEnrichmentIL7R1.24
116Aplastic anemiaEnrichmentIFNG1.24
117Autosomal non-syndromic agammaglobulinemiaEnrichmentSPI11.24
118Immune deficiency diseaseEnrichmentIKZF11.20
119Leukemia, acute lymphoblasticEnrichmentIKZF11.20
120IchthyosisEnrichmentIL2RB1.20
121Lip and oral cavity carcinomaEnrichmentKIT1.16
122Breast cancerEnrichmentIL2, IL7R1.14
123Acute promyelocytic leukemiaEnrichmentZBTB161.13
124Alzheimer's diseaseEnrichmentTNF1.13
125Isolated macular dystrophyEnrichmentITGA41.10
126Neuronal ceroid lipofuscinosisEnrichmentTPP11.07
127Myocardial infarctionEnrichmentLTA0.91
128MalariaEnrichmentTNF0.90
129Precursor t-cell acute lymphoblastic leukemiaEnrichmentZBTB160.90
130CakutEnrichmentGATA30.74
131Inherited cancer-predisposing syndromeEnrichmentKIT, RUNX10.74
132Gastric cancerEnrichmentIL1B0.65
133ThrombocytopeniaEnrichmentRUNX10.61
134Myeloma, multipleEnrichmentIL7R0.55
135Primary ovarian insufficiencyEnrichmentNOTCH20.53
136Cone-rod dystrophy 2EnrichmentITGA40.48
137Ovarian cancerEnrichmentKIT0.35
138Congenital nervous system abnormalityEnrichmentTPP10.33
139Nervous system diseaseEnrichmentTPP10.33
140Retinitis pigmentosaEnrichmentAHR0.14
141Hereditary retinal dystrophyEnrichmentITGA40.08
142Fundus dystrophyEnrichmentITGA40.08

Loading...
Loading...
Loading...