MCID: ALL026
MIFTS: 62

Allergic Hypersensitivity Disease

Categories: Immune diseases

Aliases & Classifications for Allergic Hypersensitivity Disease

MalaCards integrated aliases for Allergic Hypersensitivity Disease:

Name: Allergic Hypersensitivity Disease 12 15
Hypersensitivity 12 74 43 71
Allergic Disposition 71
Allergic Condition 71
Allergic Diseases 15
Allergic Reaction 71
Allergic Disease 12

Classifications:



External Ids:

Disease Ontology 12 DOID:1205
MeSH 43 D006967
NCIt 49 C3114
SNOMED-CT 67 418634005
ICD10 32 T78.40
UMLS 71 C0020517 C0851444 C1527304 more

Summaries for Allergic Hypersensitivity Disease

Disease Ontology : 12 An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods.

MalaCards based summary : Allergic Hypersensitivity Disease, also known as hypersensitivity, is related to hypersensitivity reaction type iii disease and hypersensitivity reaction type iv disease, and has symptoms including pruritus, nausea and vomiting and abdominal pain. An important gene associated with Allergic Hypersensitivity Disease is IL5 (Interleukin 5), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Fentanyl and Rocuronium have been mentioned in the context of this disorder. Affiliated tissues include testes, skin and t cells, and related phenotypes are hematopoietic system and digestive/alimentary

Wikipedia : 74 Hypersensitivity (also called hypersensitivity reaction or intolerance) refers to undesirable reactions... more...

Related Diseases for Allergic Hypersensitivity Disease

Diseases related to Allergic Hypersensitivity Disease via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 1915, show less)
# Related Disease Score Top Affiliating Genes
1 hypersensitivity reaction type iii disease 34.7 TNF ICOSLG CCR6
2 hypersensitivity reaction type iv disease 34.5 TNF IL4 IL2 IL10 IFNG ICOSLG
3 nut allergy 34.2 IL5 IL13 CCR6
4 bronchiolitis obliterans 33.0 TNF IL13 IL10 IFNG CXCL8
5 erythema multiforme 33.0 TNF IL5 IL4 IL2 IL13 IFNG
6 igg4-related disease 33.0 IL4 ICOSLG CCR6
7 pulmonary sarcoidosis 32.9 TNF IL2 IFNG CSF2 CCR6 CCL5
8 sarcoidosis 1 32.9 TNF IL2 IL13 IFNG ICOSLG CCR6
9 juvenile myelomonocytic leukemia 32.9 IL4 IL13 IL10 CSF2
10 alopecia areata 32.9 TNF IL4 IL2 IL13 IL10 IFNG
11 familial mediterranean fever 32.8 TNF IL10 CXCL8
12 allergic asthma 32.8 RNASE3 IL5 IL4 IL3 IL13 IL10
13 esophagitis, eosinophilic, 1 32.8 RNASE3 IL5 IL4 IL3 IL13 ICOSLG
14 bullous pemphigoid 32.7 TNF RNASE3 IL5 IL4 IL13 FCER2
15 toxicodendron dermatitis 32.6 TNF IL2 CXCL8
16 cardiac sarcoidosis 32.5 TNF IL5 IFNG CXCL8
17 mikulicz disease 32.5 IL5 IL4 IL13 IL10 CCR6
18 dermatitis, atopic 32.5 TNF RNASE3 IL5 IL4 IL2 IL13
19 cryoglobulinemia 32.5 TNF IL10 IFNG
20 autoimmune disease of cardiovascular system 32.5 TNF ICOSLG CCR6
21 autoimmune disease of exocrine system 32.5 TNF IL4 IL10 ICOSLG CCR6
22 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 32.5 IL4 IL2 IL10 ICOSLG CCR6
23 autoimmune disease of eyes, ear, nose and throat 32.4 TNF IL4 IL2 IL10 ICOSLG CCR6
24 autoimmune lymphoproliferative syndrome 32.4 TNF IL2 IL10 ICOSLG
25 autoimmune disease of blood 32.4 TNF IL5 IL4 IL2 IL10 ICOSLG
26 autoimmune disease of skin and connective tissue 32.4 TNF IL4 IL2 IL10 IFNG ICOSLG
27 autoimmune disease of endocrine system 32.4 TNF IL4 IL2 IL10 IFNG ICOSLG
28 autoimmune disease of gastrointestinal tract 32.4 TNF IL4 IL2 IL10 IFNG ICOSLG
29 ige responsiveness, atopic 32.3 RNASE3 IL5 IL4 IL13 IL10 IFNG
30 autoimmune disease of musculoskeletal system 32.3 TNF IL4 IL2 IL10 IFNG ICOSLG
31 rhinitis 32.2 TNF RNASE3 IL5 IL4 IL13 IL10
32 pollen allergy 32.1 RNASE3 IL5 IL3 IL13
33 food allergy 32.1 TNF RNASE3 IL5 IL4 IL13 IL10
34 dermatitis 32.1 TNF IL5 IL4 IL2 IL13 IL10
35 autoimmune disease of central nervous system 32.0 TNF IL5 IL4 IL2 IL13 IL10
36 allergic rhinitis 32.0 RNASE3 IL5 IL4 IL13 IL10 IFNG
37 urticaria 32.0 TNF RNASE3 IL5 IL4 IL13 IL10
38 conjunctivitis 31.7 TNF RNASE3 IL5 IL4 IL2 IL13
39 stevens-johnson syndrome/toxic epidermal necrolysis 31.7 IL5 IL2 IL13 IFNG CCR3 CCL5
40 allergic conjunctivitis 31.7 TNF RNASE3 IL5 IL4 IL2 IL13
41 interstitial lung disease 31.5 TNF IL5 IL4 IL13 IL10 IFNG
42 milk allergy 31.5 TNF RNASE3 IL5 IL4 IL13 IL10
43 cytokine deficiency 31.5 IL5 IL13
44 alopecia 31.5 TNF IL4 IL2 IFNG
45 contact dermatitis 31.4 TNF IL5 IL4 IL2 IL10 IFNG
46 leishmaniasis 31.3 TNF IL5 IL4 IL2 IL13 IL10
47 peripheral nervous system disease 31.3 TNF IL4 IL2 IL10 IFNG ICOSLG
48 irritant dermatitis 31.3 TNF IL4 CXCL8
49 bronchitis 31.3 TNF RNASE3 IL5 IL4 IL13 IL10
50 granulocytopenia 31.3 TNF IL3 CSF2
51 vernal keratoconjunctivitis 31.3 RNASE3 IL5 IL4 IL13 CCL5 CCL24
52 measles 31.3 TNF IL2 IFNG CXCL8 CCL5
53 pertussis 31.3 TNF IL10 CXCL8 CCL5 CCL11
54 pulmonary fibrosis, idiopathic 31.2 TNF IL5 IL4 IL13 IL10 IFNG
55 allergic contact dermatitis 31.2 TNF IL5 IL4 IL10 IFNG CXCL8
56 esophagitis 31.2 TNF IL5 IL4 IL13 IL10 CXCL8
57 egg allergy 31.2 IL5 IL4 IL13 IL10 CCR6
58 idiopathic interstitial pneumonia 31.2 IL4 IL13 IFNG CXCL8
59 papillary conjunctivitis 31.2 IL4 CXCL8 CCL24 CCL11
60 proteasome-associated autoinflammatory syndrome 1 31.2 TNF RNASE3 IL5 IL4 IL13 IL10
61 neutropenia 31.2 TNF IL3 IL2 IL10 IFNG CXCL8
62 autoimmune disease 31.2 TNF IL5 IL4 IL2 IL13 IL10
63 atopic keratoconjunctivitis 31.2 RNASE3 IL5 IL4 IL3 IL2 IFNG
64 rheumatic fever 31.2 TNF IL2 IL10 IFNG
65 endocarditis 31.2 TNF IL10 IFNG CXCL8
66 pneumonia 31.2 TNF IL5 IL4 IL2 IL13 IL10
67 giant papillary conjunctivitis 31.2 RNASE3 IL4 CXCL8 CCL24 CCL11
68 beta-lactam allergy 31.1 IL4 IL13 IL10
69 chronic rhinitis 31.1 RNASE3 IL5 IL4 IL13
70 exanthem 31.1 TNF IL2 IL10 IFNG ICOSLG CXCL8
71 tetanus 31.1 TNF IL5 IL4 IL2 IL13 IL10
72 extrinsic allergic alveolitis 31.1 IL10 FCER2 CXCL8 CCR6 CCL5
73 crohn's disease 31.1 TNF IL4 IL2 IL10 IFNG ICOSLG
74 thyroiditis 31.1 TNF IL4 IL2 IL10
75 syphilis 31.1 TNF IFNG CCR6
76 peritonitis 31.1 TNF IL4 IL10 IFNG CXCL8 CCL5
77 hemolytic anemia 31.1 TNF IL4 IL3 IL2 IL10 IFNG
78 fibromyalgia 31.1 TNF IL10 CXCL8
79 latex allergy 31.1 TNF RNASE3 IL5 IL4 IL13
80 candidiasis 31.1 TNF IL4 IL2 IL10 IFNG CXCL8
81 diphtheria 31.1 TNF IL5 IL4 IL3 IL2 IL13
82 purpura 31.1 TNF IL4 IL10 IFNG
83 mycosis fungoides 31.1 IL5 IL4 IL2 IFNG CCR6 CCR3
84 cystitis 31.1 TNF IL4 IL2 CXCL8
85 orchitis 31.1 TNF IL4 IL2 IL10
86 histoplasmosis 31.1 TNF IFNG CCR6
87 toxoplasmosis 31.0 TNF IL5 IL4 IL10 IFNG
88 paracoccidioidomycosis 31.0 TNF IL5 IL4 IL2 IL10 IFNG
89 typhoid fever 31.0 TNF IFNG CCR6
90 skin disease 31.0 TNF RNASE3 IL5 IL4 IL2 IL13
91 hypereosinophilic syndrome 31.0 RNASE3 IL5 IL4 IL3 IL2 IL13
92 herpes zoster 31.0 TNF IL2 IL10 IFNG ICOSLG CCR6
93 keratoconjunctivitis 31.0 TNF RNASE3 IL5 IL4 IL3 IL2
94 cutaneous leishmaniasis 31.0 TNF IL5 IL4 IL2 IL13 IL10
95 lichen planus 31.0 TNF IL4 IL2 IL10 IFNG CXCL8
96 kawasaki disease 31.0 TNF IL4 IL2 IL10
97 asthma 31.0 TNF RNASE3 IL5 IL4 IL3 IL2
98 pleurisy 31.0 TNF IL2 IFNG CXCL8
99 acquired immunodeficiency syndrome 31.0 TNF IL2 IL10 IFNG CSF2 CCR6
100 peanut allergy 31.0 IL5 IL4 IL13 IL10 IFNG ICOSLG
101 visceral leishmaniasis 31.0 TNF IL4 IL2 IL13 IL10 IFNG
102 toxocariasis 31.0 RNASE3 IL5 IL4 IL10
103 chlamydia 31.0 TNF IL5 IL4 IL10 IFNG CXCL8
104 neuritis 31.0 TNF IL4 IL10 IFNG CXCL8 CCL5
105 listeriosis 30.9 TNF IL2 IL10 ICOSLG CCR6
106 tuberculoid leprosy 30.9 IL2 IL10 IFNG CCR6
107 mumps 30.9 TNF IL2 IL10 IFNG CXCL8
108 gastritis 30.9 TNF IL10 CXCL8 CCR6 CCL5
109 burning mouth syndrome 30.9 TNF IL2 CXCL8
110 myositis 30.9 TNF IFNG ICOSLG CXCL8
111 rubella 30.9 TNF IL5 IL4 IL2 IL10 IFNG
112 vernal conjunctivitis 30.9 RNASE3 IL4 IFNG CCR6
113 lepromatous leprosy 30.9 TNF IL4 IL2 IL10 IFNG CCL17
114 poliomyelitis 30.9 TNF IL4 IL10 IFNG
115 hashimoto thyroiditis 30.9 TNF IL5 IL4 IL2 IL10 IFNG
116 chronic beryllium disease 30.9 TNF IFNG
117 ovarian cancer 30.9 TNF IL4 IL3 IL2 IL10 IFNG
118 pericarditis 30.9 TNF IFNG CXCL8
119 chagas disease 30.9 TNF IL4 IL2 IL10 IFNG CXCL8
120 chronic active epstein-barr virus infection 30.9 IL2 IL10 IFNG
121 salmonellosis 30.9 TNF IL10 IFNG CCR6
122 pulmonary edema 30.9 TNF IL13 IL10 CXCL8
123 pharyngitis 30.9 TNF CXCL8 CSF2
124 q fever 30.9 TNF IL4 IL10 IFNG CCL5
125 essential thrombocythemia 30.9 TNF IL4 IL3 CXCL8 CSF2
126 ulcerative colitis 30.9 TNF IL4 IL2 IL13 IL10 IFNG
127 trichinosis 30.8 IL5 IL4 IL3 IL13 IL10
128 irritable bowel syndrome 30.8 TNF IL10 CXCL8
129 primary biliary cirrhosis 30.8 TNF IL5 IL4 IL2 IL10 IFNG
130 dermatitis herpetiformis 30.8 TNF IL5 IL4 IL10 CXCL8 CCL11
131 cough variant asthma 30.8 RNASE3 IL5 IL4 IL13
132 amebiasis 30.8 TNF IL4 CXCL8
133 arthritis 30.8 TNF IL4 IL13 IL10 IFNG CXCL8
134 pyoderma 30.8 TNF CXCL8 CCR6
135 scabies 30.8 IL10 CXCL8 CCR6 CCL11
136 intrinsic asthma 30.8 RNASE3 IL5 IL4 IL3 IL13 FCER2
137 aseptic meningitis 30.8 TNF IL10 IFNG CXCL8
138 nickel allergic contact dermatitis 30.8 IL5 IL4 IL10 IFNG
139 otitis media 30.8 TNF RNASE3 IL5 IL4 IL2 IL13
140 immune deficiency disease 30.8 TNF IL4 IL2 IL13 IL10 IFNG
141 encephalitis 30.8 TNF IL4 IL10 CCL5
142 acute cystitis 30.8 TNF IL10 CXCL8 CCR6
143 chorioretinitis 30.8 TNF IL2 IL10 IFNG
144 chronic fatigue syndrome 30.8 TNF IL5 IL4 IL2 IL13 IL10
145 respiratory allergy 30.8 TNF RNASE3 IL5 IL4 IL3 IL13
146 bronchiolitis 30.8 TNF RNASE3 IL5 IL4 IL13 IL10
147 gastroenteritis 30.8 TNF RNASE3 IL5 IL4 IL3 IL10
148 cerebral palsy 30.8 TNF IL4 IL13 IL10 CXCL8
149 pyoderma gangrenosum 30.8 TNF CXCL8 CCR6
150 trachoma 30.8 TNF IL4 IL10
151 mycobacterium tuberculosis 1 30.8 TNF IL4 IL10 IFNG ICOSLG CCR6
152 cryptococcosis 30.8 TNF IL4 IL13 IL10 IFNG CSF2
153 ascaris lumbricoides infection 30.8 IL5 IL13 IL10 IFNG CXCL8
154 acute graft versus host disease 30.8 TNF IL4 IL2 IL10 IFNG
155 radiculopathy 30.8 IL5 IL13 IL10 CXCL8 CCL5 CCL11
156 spondylitis 30.8 TNF IL10 IFNG CCR6
157 orofacial granulomatosis 30.8 TNF IL4 IL10 IFNG CCR3 CCL5
158 intestinal schistosomiasis 30.8 IL5 IL4 IL13 IL10 ICOSLG CCR6
159 common variable immunodeficiency 30.7 TNF IL5 IL4 IL2 IL10 IFNG
160 pneumoconiosis 30.7 TNF IL4 IL10 CXCL8
161 bacterial infectious disease 30.7 TNF IL3 IL10 IFNG ICOSLG CXCL8
162 cutaneous lupus erythematosus 30.7 TNF IL10 IFNG CCL17
163 peptic ulcer disease 30.7 TNF IL10 CXCL8
164 myasthenia gravis 30.7 TNF IL4 IL2 IL10 IFNG
165 leukemia, chronic lymphocytic 30.7 TNF IL4 IL2 IL10 ICOSLG FCER2
166 myocarditis 30.7 TNF IL4 IL2 IL10 IFNG
167 pulpitis 30.7 TNF CXCL8 CCR6
168 celiac disease 1 30.7 TNF IL5 IL4 IL2 IL13 IL10
169 mucositis 30.7 IL3 IL2 IL10 CSF2
170 complex regional pain syndrome 30.7 TNF IL2 IL10 IFNG CXCL8
171 cutaneous t cell lymphoma 30.7 IL5 IL4 IL2 IFNG CCR6 CCL17
172 eales disease 30.7 TNF IL4 IL10 IFNG
173 meningoencephalitis 30.7 TNF IL4 IL10 CCR6 CCL5
174 myocardial infarction 30.7 TNF IL4 IL10 IFNG CXCL8 CCL5
175 chronic mucocutaneous candidiasis 30.7 TNF IL5 IL4 IL10 IFNG CSF2
176 nervous system disease 30.7 TNF IFNG ICOSLG CSF2 CCR6
177 diarrhea 30.7 TNF IL5 IL3 IL2 IL13 IL10
178 psoriatic arthritis 30.7 TNF IL4 IL2 IL13 IL10 IFNG
179 tonsillitis 30.7 TNF IL4 IL2 IL10 IFNG CXCL8
180 allergic bronchopulmonary aspergillosis 30.7 IL5 IL4 IL10 IFNG CCR3 CCL17
181 vaginitis 30.7 TNF IL10 CXCL8 CCR6 CCL5
182 gastroesophageal reflux 30.7 TNF IL5 IL4 CXCL8 CCR3 CCL11
183 lung disease 30.7 TNF RNASE3 IL5 IL4 IL13 IL10
184 schistosomiasis 30.7 TNF RNASE3 IL5 IL4 IL2 IL13
185 leukemia, acute myeloid 30.7 TNF IL4 IL3 IL2 IL10 IFNG
186 body mass index quantitative trait locus 11 30.7 TNF IL4 IL10 ICOSLG CXCL8 CCR6
187 systemic scleroderma 30.7 TNF IL4 IL13 IL10 IFNG ICOSLG
188 bacterial pneumonia 30.7 TNF IL10 ICOSLG CXCL8 CCR6
189 aplastic anemia 30.7 TNF IL4 IL3 IL2 IL10 IFNG
190 subacute sclerosing panencephalitis 30.7 TNF IL4 IL2 IL10 IFNG
191 severe acute respiratory syndrome 30.7 TNF IL2 IL10 IFNG CXCL8 CCL5
192 hyper ige syndrome 30.7 TNF IL4 IL13 IL10 IFNG CXCL8
193 stomatitis 30.6 TNF IL4 IL2 IL10 IFNG CXCL8
194 chronic granulomatous disease 30.6 TNF IFNG CXCL8 CSF2
195 demyelinating disease 30.6 TNF IL4 IL2 IL10 IFNG ICOSLG
196 dysentery 30.6 TNF IL10 CXCL8 CCR6
197 invasive aspergillosis 30.6 IL10 IFNG CXCL8 CCR6
198 hypertension, essential 30.6 TNF IL4 IL2 IL10 IFNG CXCL8
199 smallpox 30.6 TNF IL4 IL2 IFNG CSF2
200 hemophagocytic lymphohistiocytosis 30.6 TNF IL10 IFNG CXCL8
201 polyradiculoneuropathy 30.6 IL10 IFNG ICOSLG CCL5
202 folliculitis 30.6 TNF IL5 IL4 IFNG CCR6 CCL5
203 colitis 30.6 TNF IL4 IL2 IL13 IL10 IFNG
204 cholangitis 30.6 TNF IL2 IL10 CXCL8
205 ileitis 30.6 TNF IL10 CSF2 CCR6 CCR3 CCL5
206 metal allergy 30.6 TNF IL4 IL10
207 osteomyelitis 30.6 TNF IL4 IL13 IL10 IFNG CXCL8
208 mycoplasma pneumoniae pneumonia 30.6 TNF IL4 IL13 IL10 IFNG CSF2
209 coccidiosis 30.6 TNF IL4 IL2 IL10 IFNG ICOSLG
210 onchocerciasis 30.6 RNASE3 IL5 IL4 IL2 IL13 FCER2
211 vulvovaginitis 30.6 IL10 CXCL8 CCR6 CCL5 CCL11
212 inflammatory bowel disease 30.6 TNF IL5 IL4 IL3 IL2 IL13
213 penicillin allergy 30.6 IL4 IL13 IL10 IFNG
214 myeloma, multiple 30.6 TNF IL4 IL3 IL2 IL10 IFNG
215 aphthous stomatitis 30.6 TNF IL5 IL4 IL2 IL10 IFNG
216 common cold 30.6 TNF RNASE3 IL5 IL4 IL13 IL10
217 fruit allergy 30.6 IL5 IL4 IL13 IL10 ICOSLG CCR6
218 cellulitis 30.6 TNF RNASE3 IL5 IL4 IL2 IL10
219 chronic eosinophilic pneumonia 30.6 RNASE3 IL5 CCL5 CCL11
220 primary peritoneal carcinoma 30.6 IL10 IFNG CXCL8
221 prostatitis 30.6 TNF IL10 CXCL8
222 stachybotrys chartarum 30.6 TNF IL3 CCL5
223 cow milk allergy 30.6 TNF RNASE3 IL5 IL4 IL10
224 eczema herpeticum 30.6 IL4 IFNG CCR6
225 langerhans cell histiocytosis 30.6 IFNG CSF2 CCR6
226 pustulosis of palm and sole 30.6 TNF CXCL8 CCR6
227 carotid stenosis 30.6 TNF IL10 CXCL8
228 strongyloidiasis 30.6 IL5 IL3 IL13 IFNG CCL11
229 autoimmune vasculitis 30.6 TNF IL4 IL2 CCR6
230 graft-versus-host disease 30.5 TNF IL2 IL10 IFNG
231 connective tissue disease 30.5 TNF IL4 IL10 IFNG ICOSLG CXCL8
232 lymphoma, hodgkin, classic 30.5 IL3 IL2 IL13 ICOSLG CSF2 CCR6
233 blepharitis 30.5 TNF IL4 CCR6
234 juvenile arthritis 30.5 IL10 FCER2 CXCL8 CSF2
235 hand, foot and mouth disease 30.5 IL13 IL10 IFNG
236 silicosis 30.5 TNF IL4 IL10 CXCL8
237 staphylococcal toxic shock syndrome 30.5 TNF IFNG
238 bacterial vaginosis 30.5 TNF IL4 IL10 CXCL8
239 plasmodium falciparum malaria 30.5 TNF IL4 IL10 IFNG
240 ileus 30.5 TNF IL10 IFNG CSF2
241 histiocytosis 30.5 TNF IFNG CSF2 CCR6
242 pulmonary eosinophilia 30.5 RNASE3 IL5 IL4 IL13 CXCL8 CSF2
243 pulmonary tuberculosis 30.5 TNF IL4 IL2 IL10 IFNG
244 thrombocytopenia due to platelet alloimmunization 30.5 IL10 ICOSLG CCR6
245 proctitis 30.5 TNF RNASE3 CCR6
246 hepatitis a 30.5 TNF IL4 IL10 IFNG CXCL8
247 fixed drug eruption 30.5 IL2 IFNG
248 yellow fever 30.5 IL5 IL4 CCR6 CCL5
249 viral hepatitis 30.5 TNF IL4 IL2 IL10 IFNG
250 sudden infant death syndrome 30.5 TNF IL13 IL10 CXCL8
251 keratopathy 30.5 TNF IL4 CXCL8
252 churg-strauss syndrome 30.5 TNF RNASE3 IL5 IL3 IL2 IL10
253 mast cell neoplasm 30.5 IL3 IL2 ICOSLG
254 septic arthritis 30.5 TNF IFNG CXCL8
255 appendicitis 30.5 TNF IL2 IL10 IFNG CXCL8
256 temporal arteritis 30.5 TNF IFNG CCR6 CCL5
257 chronic inflammatory demyelinating polyradiculoneuropathy 30.5 IL10 IFNG ICOSLG CCL5
258 cheilitis 30.5 TNF CSF2 CCR6
259 periodontitis 30.5 TNF IL4 IL10 IFNG CXCL8
260 lymphoma, non-hodgkin, familial 30.5 TNF IL4 IL3 IL2 IL10 ICOSLG
261 chorioamnionitis 30.5 TNF IL4 IL10 CXCL8 CSF2
262 rosacea 30.5 TNF CXCL8 CCR6
263 progressive multifocal leukoencephalopathy 30.5 TNF IL2 ICOSLG CCR6
264 bacterial meningitis 30.5 TNF IL10 IFNG CXCL8 CSF2
265 corneal disease 30.5 TNF IL10 CXCL8 CCR6
266 juvenile rheumatoid arthritis 30.5 TNF IL2 IL10 IFNG CXCL8
267 monocytic leukemia 30.5 TNF IFNG CXCL8 CSF2
268 granulomatosis with polyangiitis 30.5 TNF IL5 ICOSLG CCR6
269 chickenpox 30.5 TNF IL4 IL2 IL10 IFNG CCR6
270 cytomegalovirus infection 30.5 TNF CXCL8 CCL5
271 reactive arthritis 30.5 TNF IL10 IFNG CXCL8 CCR6
272 filariasis 30.5 TNF IL5 IL2 IL10 IFNG CCL5
273 mucocutaneous leishmaniasis 30.5 TNF IL5 IL4 IL2 IL13 IL10
274 leptospirosis 30.5 TNF IL4 IL2 IL10 IFNG CXCL8
275 toxic shock syndrome 30.5 TNF IL4 IL2 IL10 IFNG CXCL8
276 spondyloarthropathy 30.5 TNF IL4 IL2 IL10 IFNG CCR6
277 mastitis 30.5 CXCL8 CSF2 CCR6 CCL5
278 graves' disease 30.4 IL4 IL13 IFNG ICOSLG CCL5
279 eye disease 30.4 TNF IL5 IL4 IL2 IL13 IL10
280 osteoporosis 30.4 TNF IL4 IL2 IL10 IFNG CXCL8
281 mouth disease 30.4 IL13 IL10 IFNG ICOSLG CCR6
282 uveitis 30.4 TNF IL4 IL2 IL10 IFNG CXCL8
283 arteriosclerosis 30.4 IL4 IL10 IFNG CSF2 CCL5 CCL11
284 adult respiratory distress syndrome 30.4 TNF IL10 CXCL8
285 spondyloarthropathy 1 30.4 TNF ICOSLG CCR6
286 eosinophilic gastroenteritis 30.4 RNASE3 IL5 IL4 IL3 CSF2 CCR6
287 brucellosis 30.4 TNF IL4 IL2 IL13 IL10 IFNG
288 fungal infectious disease 30.4 TNF IL5 IL4 IL2 IL13 IL10
289 myelitis 30.4 TNF IL10 ICOSLG CXCL8 CCR6 CCL11
290 status asthmaticus 30.4 RNASE3 IL5 IL13 IL10 CXCL8 CCL5
291 lymphopenia 30.4 IL4 IL2 IL10 IFNG ICOSLG CCR6
292 haemophilus influenzae 30.4 TNF CXCL8
293 intestinal disease 30.4 TNF IL10 ICOSLG CXCL8 CCR6
294 lymphadenitis 30.4 TNF IL10 IFNG ICOSLG CXCL8 CCR6
295 duodenal ulcer 30.4 TNF IL10 CXCL8
296 cervical cancer 30.4 TNF IL2 IL10 IFNG CXCL8 CCR6
297 aspergillosis 30.4 TNF IL5 IL4 IL10 IFNG CXCL8
298 dilated cardiomyopathy 30.4 TNF IL4 IL2 IL13 IL10 IFNG
299 diabetes mellitus 30.4 TNF IL4 IL2 IL10 IFNG CXCL8
300 gingivitis 30.4 TNF IL4 IL2 IL10 IFNG CXCL8
301 rheumatoid arthritis 30.4 TNF IL4 IL2 IL13 IL10 IFNG
302 herpangina 30.4 TNF IL4 IL2 IL10 IFNG ICOSLG
303 human immunodeficiency virus type 1 30.4 TNF IL2 IL10 IFNG CCR3 CCL5
304 persistent polyclonal b-cell lymphocytosis 30.4 IL4 FCER2
305 pustulosis palmaris et plantaris 30.3 TNF IL5 CCR6
306 pulmonary disease, chronic obstructive 30.3 TNF RNASE3 IL5 IL4 IL13 IL10
307 spotted fever 30.3 TNF IL10 IFNG CCL5
308 wells syndrome 30.3 RNASE3 IL5 IL2 CXCL8
309 chlamydia pneumonia 30.3 TNF IL10 CXCL8
310 vitiligo-associated multiple autoimmune disease susceptibility 1 30.3 IL2 ICOSLG CCR6
311 multidrug-resistant tuberculosis 30.3 TNF IL10 IFNG
312 trichomoniasis 30.3 TNF IL2 CXCL8
313 plasmodium vivax malaria 30.3 TNF IL2 IL10 IFNG
314 parasitic helminthiasis infectious disease 30.3 TNF RNASE3 IL5 IL4 IL3 IL2
315 myelodysplastic syndrome 30.3 TNF IL3 IL2 IL10 IFNG CXCL8
316 keratoconjunctivitis sicca 30.3 TNF IL4 CCR6
317 pleural tuberculosis 30.3 TNF IFNG CXCL8
318 bronchopneumonia 30.3 TNF IL10 CXCL8
319 eosinophilic gastritis 30.3 IL5 IL13 CCR3 CCL24 CCL11
320 atrophic gastritis 30.3 TNF IL10 CXCL8
321 scrub typhus 30.3 TNF IL10 IFNG
322 felty syndrome 30.3 IL3 CXCL8 CSF2
323 thrombocytopenia 30.3 TNF IL4 IL3 IL2 IL10 IFNG
324 autoimmune uveitis 30.3 TNF IL4 IL2 IL10 IFNG
325 uveal disease 30.3 TNF IL4 IL2 IL10 IFNG ICOSLG
326 genital herpes 30.3 IL4 IL10 CCR6 CCL5
327 vulvovaginal candidiasis 30.3 IL4 IL2 CCR6
328 leprosy 3 30.3 TNF IL5 IL4 IL2 IL10 IFNG
329 clonorchiasis 30.3 TNF IL2 IL10 IFNG CXCL8
330 bacterial sepsis 30.3 TNF IL10 CXCL8 CCR6
331 renal cell carcinoma, nonpapillary 30.3 IL4 IL2 IL13 IFNG ICOSLG CSF2
332 extrapulmonary tuberculosis 30.3 TNF IL10 IFNG
333 takayasu arteritis 30.3 TNF IL2 IL10 CCL5
334 panuveitis 30.3 TNF IL10 ICOSLG CCR6
335 rheumatic heart disease 30.3 TNF IL4 IL10
336 sialadenitis 30.3 TNF ICOSLG CCR6
337 gliosarcoma 30.3 IL4 IL2 IFNG CSF2
338 mixed connective tissue disease 30.3 TNF IL10 IFNG
339 bullous skin disease 30.3 IL5 ICOSLG CCR6 CCL5
340 anemia, autoimmune hemolytic 30.3 IL2 ICOSLG CCR6
341 secondary progressive multiple sclerosis 30.3 IL4 IL10 IFNG CCR6 CCR3
342 crohn's colitis 30.3 TNF IL2 IFNG CXCL8 CCR6
343 immunodeficiency with hyper-igm, type 1 30.2 IL4 ICOSLG CCR6
344 pulmonary alveolar proteinosis 30.2 TNF IL3 IL10 CXCL8 CSF2
345 systemic lupus erythematosus 30.2 TNF IL5 IL4 IL2 IL13 IL10
346 pyelonephritis 30.2 TNF IL10 IFNG CXCL8 CCL5
347 dengue hemorrhagic fever 30.2 TNF IL4 IL13 IL10 IFNG CXCL8
348 coronavirus infectious disease 30.2 TNF CXCL8 CCR6
349 echinococcosis 30.2 TNF RNASE3 IL5 IL10 IFNG CCL17
350 meningitis 30.2 TNF IL5 IL4 IL2 IL13 IL10
351 t-cell lymphoblastic leukemia/lymphoma 30.2 IL5 IL3 IL2 CCR6
352 engraftment syndrome 30.2 CXCL8 CSF2
353 legume allergy 30.2 IL5 IL4 IL13 IL10 ICOSLG CCR6
354 retinal detachment 30.2 TNF IL10 IFNG CXCL8
355 eosinophilic meningitis 30.2 IL5 IL4 IL2 IL13 IL10 CCL24
356 eosinophilic pneumonia 30.2 RNASE3 IL5 IL4 IL3 IL13 CXCL8
357 neurosyphilis 30.2 IL10 CXCL8
358 urinary schistosomiasis 30.2 RNASE3 IL5 IL4 IL13 IL10 IFNG
359 severe combined immunodeficiency 30.2 IL5 IL4 IL3 IL2 IL13 IL10
360 b cell deficiency 30.2 TNF IL4 IL2 IL10 ICOSLG CCR6
361 ceftriaxone allergy 30.2 IL5 IL13
362 central nervous system disease 30.2 TNF IFNG ICOSLG CCR6
363 respiratory failure 30.2 TNF RNASE3 IL5 IL13 IL10 CXCL8
364 muckle-wells syndrome 30.2 TNF CXCL8 CCR6
365 malaria 30.2 TNF RNASE3 IL5 IL4 IL3 IL2
366 blood platelet disease 30.2 TNF IL3 IL2 ICOSLG CSF2 CCR6
367 diabetes mellitus, type i 30.1 TNF IL5 IL4 IL2 IL13 IL10
368 bone disease 30.1 TNF IL4 IL3 ICOSLG CXCL8 CCR6
369 alcoholic liver cirrhosis 30.1 TNF IL10 CXCL8
370 psoriasis 30.1 TNF IL5 IL4 IL2 IL13 IL10
371 diabetes mellitus, noninsulin-dependent 30.1 TNF IL4 IL10 ICOSLG CXCL8 CCR6
372 omenn syndrome 30.1 TNF IL5 IL4 IL2 IL10 IFNG
373 viral infectious disease 30.1 TNF IL4 IL2 IL13 IL10 IFNG
374 hematologic cancer 30.1 TNF IL3 IL2 ICOSLG CSF2 CCR6
375 alcoholic hepatitis 30.0 TNF IL10 CXCL8
376 multiple sclerosis 30.0 TNF IL5 IL4 IL2 IL13 IL10
377 adult t-cell leukemia 29.9 IL2 CCR6 CCL17
378 parasitic protozoa infectious disease 29.9 TNF IL5 IL4 IL2 IL13 IL10
379 diclofenac allergy 29.8 IL3 CCR3
380 acute promyelocytic leukemia 29.6 TNF IL3 IL10 CXCL8 CSF2
381 hypersensitivity vasculitis 12.8
382 hypersensitivity pneumonitis, familial 12.6
383 insect stings, hypersensitivity to 12.3
384 asparagus, specific smell hypersensitivity 12.2
385 allergic cutaneous vasculitis 11.8
386 familial cold autoinflammatory syndrome 1 11.7
387 severe cutaneous adverse reaction 11.7
388 bird fancier's lung 11.7
389 wheat allergy 11.6
390 familial cold autoinflammatory syndrome 11.6
391 arthus reaction 11.5
392 bagassosis 11.5
393 erythrocytosis, familial, 1 11.5
394 drug reaction with eosinophilia and systemic symptoms 11.5
395 idiopathic infantile hypercalcemia 11.4
396 fanconi anemia, complementation group a 11.4
397 fanconi anemia, complementation group c 11.4
398 fanconi anemia, complementation group d2 11.4
399 nijmegen breakage syndrome 11.4
400 fanconi anemia, complementation group b 11.4
401 fanconi anemia, complementation group e 11.4
402 fanconi anemia, complementation group d1 11.4
403 fanconi anemia, complementation group n 11.4
404 fanconi anemia, complementation group o 11.4
405 fanconi anemia, complementation group g 11.4
406 goodpasture syndrome 11.3
407 mushroom workers' lung 11.3
408 xeroderma pigmentosum, variant type 11.3
409 polycythemia vera 11.3
410 beryllium disease 11.3
411 bruxism 11.3
412 sjogren syndrome 11.3
413 xeroderma pigmentosum, complementation group a 11.3
414 hypercalcemia, infantile, 1 11.2
415 enhanced s-cone syndrome 11.2
416 xeroderma pigmentosum, complementation group d 11.2
417 cinca syndrome 11.2
418 fanconi anemia, complementation group u 11.2
419 vogt-koyanagi-harada disease 11.2
420 antiphospholipid syndrome 11.2
421 photoallergic dermatitis 11.2
422 subacute bacterial endocarditis 11.2
423 gianotti crosti syndrome 11.2
424 heiner syndrome 11.1
425 erythrocytosis, familial, 2, autosomal recessive 11.1
426 fanconi anemia, complementation group f 11.1
427 fanconi anemia, complementation group i 11.1
428 fanconi anemia, complementation group j 11.1
429 fanconi anemia, complementation group l 11.1
430 fanconi anemia, complementation group q 11.1
431 jansen-de vries syndrome 11.1
432 eosinophil peroxidase deficiency 11.0
433 selective igm deficiency disease 11.0
434 pemphigus vulgaris, familial 10.9
435 carboxypeptidase n deficiency 10.9
436 xeroderma pigmentosum, complementation group c 10.9
437 xeroderma pigmentosum, complementation group e 10.9
438 xeroderma pigmentosum, complementation group f 10.9
439 xeroderma pigmentosum, complementation group g 10.9
440 ataxia-telangiectasia-like disorder 1 10.9
441 xeroderma pigmentosum, complementation group b 10.9
442 warsaw breakage syndrome 10.9
443 tuberculin skin test reactivity, absence of 10.9
444 tuberculin skin test reactivity quantitative trait locus 10.9
445 fanconi anemia, complementation group p 10.9
446 fanconi anemia, complementation group t 10.9
447 fanconi anemia, complementation group v 10.9
448 fanconi anemia, complementation group r 10.9
449 fanconi anemia, complementation group w 10.9
450 fanconi anemia, complementation group s 10.9
451 autoimmune disease of urogenital tract 10.9
452 heavy chain disease 10.9
453 sting-associated vasculopathy with onset in infancy 10.9
454 paranoid personality disorder 10.9
455 phlyctenulosis 10.9
456 sympathetic ophthalmia 10.9
457 atypical depressive disorder 10.9
458 jaccoud's syndrome 10.9
459 neurosarcoidosis 10.9
460 uveoparotid fever 10.9
461 dipetalonemiasis 10.9
462 schnitzler syndrome 10.9
463 chronic nk-cell lymphocytosis 10.9
464 tropical endomyocardial fibrosis 10.8 TNF IL4 IL10
465 aztreonam allergy 10.8 IL5 IL2 IL13
466 angioimmunoblastic lymphadenopathy with dysproteinemia 10.8 TNF IL5 IL13
467 1-chloro-2,4-dinitrobenzene allergic contact dermatitis 10.8 IL4 IL2
468 punctate inner choroidopathy 10.8 TNF IL10
469 loeffler endocarditis 10.8 RNASE3 IL5 IL3
470 b-cell growth factor 10.8 IL4 IL3 IFNG
471 loeffler syndrome 10.8 IL5 IL13 CCR3
472 respiratory syncytial virus infectious disease 10.8 IL5 IL13 CCL5
473 pemphigoid gestationis 10.8 RNASE3 IL5 CCL11
474 chronic meningitis 10.8 IL5 IL13 CCL11
475 loiasis 10.8 IL5 IL4 IL13 IL10
476 eosinophilic fasciitis 10.8 IL5 IFNG
477 toxic oil syndrome 10.8 IL5 IL4 IFNG FCER2
478 streptococcal toxic-shock syndrome 10.8 TNF IL2 CXCL8
479 filarial elephantiasis 10.8 IL5 IL4 IL13 IL10
480 oral tuberculosis 10.8 TNF IL2 IFNG
481 taeniasis 10.8 TNF IL4 IL10
482 scorpion envenomation 10.8 TNF CCL5
483 choroiditis 10.8 TNF IL10 IFNG
484 macs syndrome 10.8 TNF IL10 IFNG
485 transverse myelitis 10.8 TNF IL10 CXCL8
486 microscopic colitis 10.8 TNF IL4 IL2 IFNG
487 paragonimiasis 10.8 RNASE3 IL5 IL13 CCL17
488 cardiomyopathy, familial hypertrophic, 20 10.8 TNF IL13 CXCL8
489 spotted fever rickettsiosis 10.8 TNF IL10 IFNG CCL5
490 progressive myoclonus epilepsy 8 10.8 TNF IL10 CXCL8
491 elephantiasis 10.8 RNASE3 IL5 IL4 IL13 IL10
492 endomyocardial fibrosis 10.8 TNF RNASE3 IL5 IL4 IL10
493 funisitis 10.8 TNF IL10 CXCL8
494 opisthorchiasis 10.8 TNF IL4 CXCL8
495 central nervous system vasculitis 10.8 TNF IFNG CCR6
496 disseminated eosinophilic collagen disease 10.8 RNASE3 IL5 IL3 CCL17
497 trichuriasis 10.8 TNF IL13 IL10 CXCL8
498 paratyphoid fever 10.8 TNF IFNG CCR6
499 cytomegalovirus retinitis 10.8 TNF IL10 IFNG CSF2
500 scleral disease 10.8 TNF IL2 IFNG CCR6
501 drug-induced lupus erythematosus 10.8 TNF IL4 IL10 CXCL8
502 multicentric castleman disease 10.8 IL5 IL10 IFNG
503 mycetoma 10.8 IL10 CXCL8 CCL5
504 mucormycosis 10.8 IFNG CSF2 CCR6
505 palladium allergic contact dermatitis 10.8 TNF IL10 CSF2 CCL17
506 virus associated hemophagocytic syndrome 10.8 IL4 IL2
507 cervicitis 10.8 TNF IL2 CXCL8
508 relapsing polychondritis 10.8 IL2 IL10 IFNG CXCL8
509 dental pulp disease 10.8 TNF CXCL8 CCR6
510 idiopathic neutropenia 10.8 TNF IL10 FCER2 CCL5
511 hypersplenism 10.8 IL4 IFNG CSF2
512 meconium aspiration syndrome 10.7 TNF IFNG CXCL8 CSF2
513 aggressive periodontitis 10.7 TNF IL4 IL10 CXCL8
514 b-cell expansion with nfkb and t-cell anergy 10.7 IL2 FCER2 CCL5
515 autoimmune myocarditis 10.7 TNF IFNG
516 endometrial disease 10.7 TNF IL10 CXCL8
517 multifocal choroiditis 10.7 TNF IL10
518 scleritis 10.7 TNF IL5 IL4 IFNG CCR6
519 periapical granuloma 10.7 IL4 IL2 CXCL8 CCL5
520 fasciitis 10.7 TNF IL2 IFNG CXCL8
521 idiopathic anterior uveitis 10.7 TNF CXCL8
522 blau syndrome 10.7 TNF IL4 IL10
523 primary progressive multiple sclerosis 10.7 TNF IL4 IL10 CCR6
524 acute proliferative glomerulonephritis 10.7 TNF ICOSLG CCR6
525 cecal disease 10.7 TNF CXCL8 CCR6
526 streptococcus pneumonia 10.7 TNF IL10 CXCL8 CCR6
527 central nervous system lymphoma 10.7 TNF IL2 IL10 CCR6
528 gingival disease 10.7 TNF IL10 CXCL8 CCR6
529 african tick-bite fever 10.7 TNF IL13 IL10 IFNG CCL5
530 tropical spastic paraparesis 10.7 IL2 IL10 IFNG CCL5
531 cryptococcal meningitis 10.7 IFNG CSF2 CCR6
532 pyelitis 10.7 TNF CXCL8 CCR6
533 perinatal necrotizing enterocolitis 10.7 TNF IL10 CXCL8 CCR6
534 middle ear disease 10.7 TNF IL10 CXCL8 CCR6
535 childhood type dermatomyositis 10.7 TNF ICOSLG CCR6
536 localized scleroderma 10.7 TNF IL4 IL2 IL13 CCL5
537 primary thrombocytopenia 10.7 IL10 ICOSLG CCR6
538 fallopian tube disease 10.7 TNF CXCL8 CCR6
539 autoimmune disease of peripheral nervous system 10.7 TNF IL10 ICOSLG CCR6
540 capillary disease 10.7 IL2 ICOSLG CSF2
541 acute pyelonephritis 10.7 IL10 IFNG CXCL8
542 cefaclor allergy 10.7 IL5 IL13
543 severe combined immunodeficiency, x-linked 10.7 IL4 IL2 IL13
544 sclerosing cholangitis 10.7 TNF IL2 IL10 CXCL8
545 intermediate uveitis 10.7 TNF IL2 IL10 IFNG CCR6
546 angiostrongyliasis 10.7 IL5 IL4 IL2 IL13 CCL24 CCL11
547 capillary leak syndrome 10.7 IL2 ICOSLG CXCL8 CSF2
548 pleural disease 10.7 TNF IFNG CXCL8 CCR6
549 dacryoadenitis 10.7 IL4 IL13 IL10 ICOSLG CCR6
550 polyarticular juvenile idiopathic arthritis 10.7 TNF IFNG
551 viral meningitis 10.7 IFNG CXCL8 CCL5
552 severe congenital neutropenia 10.7 TNF IL3 IL2 CSF2
553 cyclic neutropenia 10.7 TNF IL3 IFNG CXCL8 CSF2
554 mansonelliasis 10.7 CCL24 CCL17
555 t cell deficiency 10.7 IL2 ICOSLG CCR6
556 chediak-higashi syndrome 10.7 IL4 IL10 ICOSLG CCR6
557 acute transverse myelitis 10.7 IL10 CXCL8
558 sebaceous gland disease 10.7 TNF CXCL8 CCR6
559 preterm premature rupture of the membranes 10.7 TNF IL10 CXCL8
560 cefuroxime allergy 10.7 IL5 IL13
561 viral pneumonia 10.7 TNF IL10 CXCL8 CCR6 CCL5
562 melioidosis 10.7 TNF IL10 IFNG
563 splenic disease 10.7 TNF IL4 IL2 IL10 IFNG CCR6
564 potocki-shaffer syndrome 10.7 TNF IL4 IL10 ICOSLG CCR6
565 fungal meningitis 10.7 TNF IL4 IL10 IFNG CSF2 CCR6
566 spinal cord disease 10.7 TNF IL2 IL10 ICOSLG CCR6
567 castleman disease 10.7 IL5 IL4 IL10 IFNG CXCL8 CSF2
568 agammaglobulinemia, x-linked 10.7 IL4 IL2 ICOSLG
569 cholangitis, primary sclerosing 10.7 TNF IL10 ICOSLG CCR6
570 salivary gland disease 10.7 TNF IL2 IL10 ICOSLG CCR6
571 monoclonal gammopathy of uncertain significance 10.7 TNF ICOSLG CCR6
572 viral encephalitis 10.7 TNF IL10 CXCL8 CCR6 CCL5
573 testicular disease 10.7 TNF IL4 IL2 IL10 IFNG CCR6
574 vein disease 10.7 TNF CXCL8 CCR6
575 thymus gland disease 10.7 IL2 ICOSLG CCR6
576 pelvic inflammatory disease 10.7 IL2 IL13 IFNG
577 thymus cancer 10.7 IL2 ICOSLG CCR6
578 x-linked monogenic disease 10.7 TNF IL2 IL10 ICOSLG CCR6
579 stomach disease 10.7 TNF IL10 ICOSLG CXCL8 CCR6
580 obstructive jaundice 10.7 TNF IL2 CXCL8
581 kimura disease 10.7 RNASE3 IL5 IL4 IL13 CCR3 CCL5
582 bone marrow cancer 10.7 IL3 ICOSLG CSF2 CCR6
583 jak3-deficient severe combined immunodeficiency 10.7 IL4 IL2
584 hypotrichosis 1 10.7 TNF IL4 IL2 IL10 ICOSLG CCR6
585 extrinsic cardiomyopathy 10.7 TNF IL4 IL2 IL10 ICOSLG CCR6
586 hair disease 10.7 TNF IL4 IL2 IL10 ICOSLG CCR6
587 lacrimal apparatus disease 10.7 TNF IL4 IL10 ICOSLG CXCL8 CCR6
588 overnutrition 10.7 TNF IL10 ICOSLG CCR6
589 x-linked recessive disease 10.7 TNF IL4 IL2 IL10 ICOSLG CCR6
590 optic neuritis 10.7 TNF IL10 CXCL8
591 chronic graft versus host disease 10.7 IL10 IFNG
592 vaginal disease 10.7 TNF IL2 IL10 CXCL8 CCR6 CCL5
593 primary systemic mycosis 10.7 TNF IL4 IL2 IL10 IFNG CSF2
594 anus disease 10.7 TNF IL2 IL10 ICOSLG CXCL8 CCR6
595 rectal disease 10.7 TNF IL2 IL10 ICOSLG CXCL8 CCR6
596 dengue disease 10.7 TNF ICOSLG CCL5
597 fuchs' heterochromic uveitis 10.7 IFNG CXCL8
598 glucose metabolism disease 10.6 TNF IL10 ICOSLG CCR6
599 narcolepsy 10.6 TNF IL2 CXCL8 CCR3
600 sezary's disease 10.6 IL5 IL4 IL2 IL10 IFNG CCR6
601 autoimmune gastritis 10.6 TNF IL4 IL2 IL10 IFNG ICOSLG
602 trypanosomiasis 10.6 TNF IL4 IL2 IL10 IFNG CXCL8
603 shigellosis 10.6 TNF IL10 CXCL8
604 lymph node disease 10.6 TNF IL4 IL2 IL10 IFNG ICOSLG
605 acquired metabolic disease 10.6 TNF IL10 ICOSLG CCR6
606 autosomal genetic disease 10.6 TNF ICOSLG CXCL8 CCR6
607 kidney cancer 10.6 TNF IL2 IFNG ICOSLG CXCL8 CSF2
608 immune system disease 10.6 TNF IL4 IL2 IL13 IL10 ICOSLG
609 posterior uveitis 10.6 TNF IL5 IL4 IL2 IL13 IFNG
610 cranial nerve disease 10.6 TNF ICOSLG CCR6
611 blood coagulation disease 10.6 TNF IL3 IL2 IL10 ICOSLG CSF2
612 lichen disease 10.6 TNF IL4 IL2 IL10 IFNG ICOSLG
613 autoimmune hepatitis type 1 10.6 IL4 IL10
614 commensal bacterial infectious disease 10.6 TNF IL5 IL4 IL2 IL10 IFNG
615 ventilation pneumonitis 10.6
616 malt worker's lung 10.6
617 cork-handlers' disease 10.6
618 mature b-cell neoplasm 10.6 IL2 ICOSLG CCR6
619 gingival overgrowth 10.5 TNF IL2 CXCL8
620 relapsing-remitting multiple sclerosis 10.5 TNF IL4 IL2 IL10 IFNG CXCL8
621 candida glabrata 10.5 IFNG CSF2
622 asthma-related traits 4 10.5
623 paranasal sinus disease 10.5 TNF RNASE3 IL5 IL4 IL13 IL10
624 pulmonary fibrosis 10.5
625 aids dementia complex 10.5 TNF CCR3
626 bone inflammation disease 10.5 TNF IL4 IL2 IL13 IL10 IFNG
627 combined t cell and b cell immunodeficiency 10.5 TNF IL4 IL3 IL2 IL10 IFNG
628 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 10.5
629 human immunodeficiency virus infectious disease 10.5 TNF IL4 IL2 IL10 IFNG ICOSLG
630 upper respiratory tract disease 10.5 TNF RNASE3 IL5 IL4 IL2 IL13
631 anaerobic pneumonia 10.5 TNF CCL5
632 chronic conjunctivitis 10.5 TNF RNASE3 IL5 IL4 IL13 IL10
633 erythema multiforme major 10.5
634 chronic pain 10.5
635 opportunistic mycosis 10.5 TNF IL5 IL4 IL2 IL13 IL10
636 skin sarcoidosis 10.5 TNF IL2
637 leukocyte disease 10.4 TNF IL5 IL4 IL3 IL2 IL13
638 conjunctival disease 10.4 TNF RNASE3 IL5 IL4 IL2 IL13
639 behcet syndrome 10.4 TNF IL5 IL4 IL2 IL13 IL10
640 primary bacterial infectious disease 10.4 TNF IL5 IL4 IL2 IL13 IL10
641 integumentary system disease 10.4 TNF IL5 IL4 IL2 IL13 IL10
642 neutropenia, severe congenital, 3, autosomal recessive 10.4 IL3 CSF2
643 neuropathy 10.4
644 gingival recession 10.4
645 house allergic alveolitis 10.3
646 ataxia and polyneuropathy, adult-onset 10.3
647 hypereosinophilic syndrome, idiopathic 10.3 IL5 IL3
648 telangiectasis 10.3
649 ataxia-telangiectasia 10.3
650 drug allergy 10.3
651 leukemia, acute lymphoblastic 10.3
652 interstitial nephritis 10.3
653 herpes simplex 10.3
654 nonspecific interstitial pneumonia 10.3
655 kala-azar 1 10.2
656 fibrosis of extraocular muscles, congenital, 1 10.2
657 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.2
658 spinal cord injury 10.2
659 acute kidney failure 10.2
660 ischemia 10.2
661 vaccinia 10.2
662 bronchiectasis 10.2
663 maple bark strippers' lung 10.2
664 angioedema 10.2
665 cystic fibrosis 10.2
666 nose disease 10.2 TNF RNASE3 IL5 IL4 IL3 IL2
667 nasal cavity disease 10.2 TNF RNASE3 IL5 IL4 IL3 IL2
668 erythroleukemia, familial 10.2
669 rickets 10.2
670 autism 10.2
671 headache 10.2
672 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.2
673 leukemia 10.1
674 exfoliative dermatitis 10.1
675 breast cancer 10.1
676 kidney disease 10.1
677 acute generalized exanthematous pustulosis 10.1
678 bronchial disease 10.1 TNF RNASE3 IL5 IL4 IL3 IL2
679 cholera 10.1
680 deficiency anemia 10.1
681 hepatitis 10.1
682 gout 10.1
683 hyperuricemia 10.1
684 fibrosarcoma 10.1
685 skin carcinoma 10.1
686 panic disorder 10.1
687 dentin sensitivity 10.1
688 whiplash 10.1
689 hair whorl 10.1
690 collagen disease 10.1
691 colorectal cancer 10.1
692 thalassemia 10.1
693 melanoma 10.0
694 cockayne syndrome 10.0
695 myeloid leukemia 10.0
696 attention deficit-hyperactivity disorder 10.0
697 migraine with or without aura 1 10.0
698 enthesopathy 10.0
699 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 10.0
700 lymphocytic choriomeningitis 10.0
701 bone cancer 10.0
702 iron metabolism disease 10.0
703 rapidly involuting congenital hemangioma 10.0
704 bladder cancer 10.0
705 osteogenic sarcoma 10.0
706 atrioventricular block 10.0
707 polyneuropathy 10.0
708 hyperthyroidism 10.0
709 hyperacusis 10.0
710 immunoglobulin e concentration, serum 10.0
711 triiodothyronine receptor auxiliary protein 10.0
712 body mass index quantitative trait locus 1 10.0
713 mastocytosis 10.0
714 tardive dyskinesia 10.0
715 melanoma, cutaneous malignant 10 10.0
716 hyperlipoproteinemia, type iii 10.0
717 lipoprotein quantitative trait locus 10.0
718 cardiac arrest 10.0
719 cholestasis 10.0
720 myeloproliferative neoplasm 10.0
721 iridocyclitis 10.0
722 pure autonomic failure 10.0
723 pulmonary hypertension 10.0
724 guillain-barre syndrome 10.0
725 liver disease 10.0
726 congestive heart failure 10.0
727 polycythemia 10.0
728 dermatophytosis 10.0
729 hydroa vacciniforme 10.0
730 encephalopathy 10.0
731 helicobacter pylori infection 10.0
732 immunoglobulin alpha deficiency 10.0
733 constipation 10.0
734 vasculitis 10.0
735 beta-thalassemia 10.0
736 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 10.0
737 berylliosis 10.0
738 lactose intolerance 10.0
739 disseminated intravascular coagulation 10.0
740 rabies 10.0
741 mononeuropathy 10.0
742 embryonal carcinoma 10.0
743 heparin-induced thrombocytopenia 10.0
744 back pain 10.0
745 pancreatic cancer 9.9
746 leukemia, chronic myeloid 9.9
747 cyanosis, transient neonatal 9.9
748 glucocorticoid resistance, generalized 9.9
749 angina pectoris 9.9
750 corticosteroid allergy 9.9
751 pain agnosia 9.9
752 low compliance bladder 9.9
753 sick sinus syndrome 9.9
754 newcastle disease 9.9
755 dysphagia 9.9
756 body mass index quantitative trait locus 9 9.9
757 body mass index quantitative trait locus 8 9.9
758 body mass index quantitative trait locus 4 9.9
759 body mass index quantitative trait locus 10 9.9
760 body mass index quantitative trait locus 7 9.9
761 body mass index quantitative trait locus 12 9.9
762 body mass index quantitative trait locus 14 9.9
763 body mass index quantitative trait locus 18 9.9
764 body mass index quantitative trait locus 19 9.9
765 body mass index quantitative trait locus 20 9.9
766 arteries, anomalies of 9.9
767 neutrophil migration 9.9
768 dowling-degos disease 1 9.9
769 autosomal recessive disease 9.9
770 iron deficiency anemia 9.9
771 migraine without aura 9.9
772 coccidioidomycosis 9.9
773 personality disorder 9.9
774 granulomatous hepatitis 9.9
775 endometriosis 9.9
776 glioblastoma multiforme 9.9
777 hyperglycemia 9.9
778 anthrax disease 9.9
779 malignant hyperthermia 9.9
780 neurofibromatosis 9.9
781 pulmonary embolism 9.9
782 sickle cell disease 9.9
783 oral lichen planus 9.9
784 alcohol dependence 9.9
785 alzheimer disease 9.9
786 burkitt lymphoma 9.9
787 hpa i recognition polymorphism, beta-globin-related 9.9
788 trigeminal neuralgia 9.9
789 sickle cell anemia 9.9
790 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 9.9
791 peripheral vascular disease 9.9
792 infective endocarditis 9.9
793 sarcoma 9.9
794 erysipelas 9.9
795 plica syndrome 9.9
796 pancytopenia 9.9
797 blastomycosis 9.9
798 dental caries 9.9
799 synovitis 9.9
800 astrocytoma 9.9
801 spindle cell sarcoma 9.9
802 uremia 9.9
803 acute myocardial infarction 9.9
804 diabetic neuropathy 9.9
805 muscular dystrophy 9.9
806 tremor 9.9
807 acute liver failure 9.9
808 cardiogenic shock 9.9
809 neurofibromatosis, type ii 9.9
810 schistosoma mansoni infection, susceptibility/ 9.9
811 interstitial cystitis 9.9
812 mood disorder 9.9
813 multiple chemical sensitivity 9.9
814 sleep disorder 9.9
815 allergic encephalomyelitis 9.9
816 pik3ca-related overgrowth syndrome 9.9
817 overgrowth syndrome 9.9
818 atrial standstill 1 9.8
819 huntington disease 9.8
820 kaposi sarcoma 9.8
821 keratitis, hereditary 9.8
822 retinoblastoma 9.8
823 schizophrenia 9.8
824 suppressor of tumorigenicity 3 9.8
825 bloom syndrome 9.8
826 graves disease 1 9.8
827 paine syndrome 9.8
828 branchiootic syndrome 1 9.8
829 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.8
830 helix syndrome 9.8
831 borderline personality disorder 9.8
832 autonomic neuropathy 9.8
833 protein-energy malnutrition 9.8
834 squamous cell papilloma 9.8
835 mental depression 9.8
836 keratosis 9.8
837 sensory peripheral neuropathy 9.8
838 papilloma 9.8
839 adenocarcinoma 9.8
840 myopathy 9.8
841 spongiotic dermatitis 9.8
842 familial retinoblastoma 9.8
843 b-cell lymphoma 9.8
844 neuroblastoma 9.8
845 osteoarthritis 9.8
846 trichorhinophalangeal syndrome 9.8
847 autoimmune progesterone dermatitis 9.8
848 microscopic polyangiitis 9.8
849 posttransplant acute limbic encephalitis 9.8
850 amyotrophic lateral sclerosis 1 9.8
851 thrombophilia due to thrombin defect 9.8
852 down syndrome 9.8
853 acetylation, slow 9.8
854 thymoma, familial 9.8
855 muscular dystrophy, duchenne type 9.8
856 dermatitis herpetiformis, familial 9.8
857 major depressive disorder 9.8
858 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.8
859 gastrointestinal ulceration, recurrent, with dysfunctional platelets 9.8
860 lymphoblastic lymphoma 9.8
861 neuroretinitis 9.8
862 japanese encephalitis 9.8
863 hemopericardium 9.8
864 pericardial effusion 9.8
865 coronary artery vasospasm 9.8
866 hypertrophic cardiomyopathy 9.8
867 acute kidney tubular necrosis 9.8
868 dermatomycosis 9.8
869 squamous cell carcinoma 9.8
870 cholecystitis 9.8
871 drug-induced hepatitis 9.8
872 lateral sclerosis 9.8
873 thymoma 9.8
874 retinitis 9.8
875 arthropathy 9.8
876 shwartzman phenomenon 9.8
877 intermediate coronary syndrome 9.8
878 fatty liver disease 9.8
879 anca-associated vasculitis 9.8
880 mast cell activation syndrome 9.8
881 ovarian epithelial cancer 9.8
882 raynaud phenomenon 9.8
883 head injury 9.8
884 hypoxia 9.8
885 virus-associated trichodysplasia spinulosa 9.8
886 atherosclerosis susceptibility 9.8
887 gilles de la tourette syndrome 9.8
888 pulmonary hemosiderosis 9.8
889 neural tube defects 9.8
890 enterocolitis 9.8
891 meningioma, radiation-induced 9.8
892 meningioma, familial 9.8
893 anxiety 9.8
894 dermatitis, atopic, 8 9.8
895 ectodermal dysplasia-syndactyly syndrome 2 9.8
896 sleep apnea 9.8
897 oppositional defiant disorder 9.8
898 physical urticaria 9.8
899 adenoid hypertrophy 9.8
900 covid-19 9.8
901 keratoconus 9.8
902 glucose intolerance 9.8
903 allergic urticaria 9.8
904 spinal meningioma 9.8
905 nephrotic syndrome 9.8
906 inflammatory spondylopathy 9.8
907 hemosiderosis 9.8
908 agammaglobulinemia 9.8
909 glomerulonephritis 9.8
910 ascaridiasis 9.8
911 laryngitis 9.8
912 occupational dermatitis 9.8
913 secretory meningioma 9.8
914 lymphoplasmacyte-rich meningioma 9.8
915 liver cirrhosis 9.8
916 anisakiasis 9.8
917 gastrointestinal system disease 9.8
918 lupus erythematosus 9.8
919 pulmonary emphysema 9.8
920 bacterial conjunctivitis 9.8
921 48,xyyy 9.8
922 glioma 9.8
923 glial tumor 9.8
924 hepatocellular carcinoma 9.8
925 motion sickness 9.8
926 parkinson disease, late-onset 9.8
927 volvulus of midgut 9.8
928 neuropathy, hereditary sensory and autonomic, type iii 9.8
929 halothane hepatitis 9.8
930 ocular motor apraxia 9.8
931 resting heart rate, variation in 9.8
932 bone mineral density quantitative trait locus 8 9.8
933 bone mineral density quantitative trait locus 15 9.8
934 dengue virus 9.8
935 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.8
936 cephalosporin allergy 9.8
937 pulmonary aspergilloma 9.8
938 cryptogenic organizing pneumonia 9.8
939 trichosporonosis 9.8
940 hypophosphatemia 9.8
941 mantle cell lymphoma 9.8
942 sinoatrial node disease 9.8
943 atrial fibrillation 9.8
944 osteonecrosis 9.8
945 anthracosis 9.8
946 dentin caries 9.8
947 heart disease 9.8
948 polycystic ovary syndrome 9.8
949 goiter 9.8
950 tinea pedis 9.8
951 acute leukemia 9.8
952 crescentic glomerulonephritis 9.8
953 porphyria 9.8
954 iritis 9.8
955 panniculitis 9.8
956 status epilepticus 9.8
957 hypogonadism 9.8
958 hyperinsulinism 9.8
959 tularemia 9.8
960 basal cell carcinoma 9.8
961 teratocarcinoma 9.8
962 inappropriate adh syndrome 9.8
963 mammary paget's disease 9.8
964 plasmacytoma 9.8
965 demyelinating polyneuropathy 9.8
966 chronic kidney disease 9.8
967 retinal degeneration 9.8
968 ocular hypertension 9.8
969 chromosomal triplication 9.8
970 exercise-induced anaphylaxis 9.8
971 mycobacterium chelonae 9.8
972 ocular toxoplasmosis 9.8
973 autonomic dysfunction 9.8
974 dysautonomia 9.8
975 myoclonus 9.8
976 traumatic brain injury 9.8
977 premature aging 9.8
978 thyroid carcinoma 9.8
979 basal cell nevus syndrome 9.7
980 cardiac conduction defect 9.7
981 glaucoma, primary open angle 9.7
982 neutrophilia, hereditary 9.7
983 nevus anemicus 9.7
984 pheochromocytoma 9.7
985 vasculitis, lymphocytic, nodular 9.7
986 periodontitis, chronic 9.7
987 retinitis pigmentosa 9.7
988 roberts syndrome 9.7
989 insulin-like growth factor i 9.7
990 fragile x syndrome 9.7
991 aging 9.7
992 cd4/cd8 t-cell ratio 9.7
993 macular degeneration, age-related, 1 9.7
994 nasopharyngeal carcinoma 9.7
995 neutrophilic dermatosis, acute febrile 9.7
996 endometrial cancer 9.7
997 fanconi renotubular syndrome 2 9.7
998 mucopolysaccharidosis-plus syndrome 9.7
999 shrimp allergy 9.7
1000 tick-borne encephalitis 9.7
1001 variola major 9.7
1002 adrenal gland pheochromocytoma 9.7
1003 pervasive developmental disorder 9.7
1004 alexithymia 9.7
1005 apple allergy 9.7
1006 peach allergy 9.7
1007 childhood acute lymphocytic leukemia 9.7
1008 chronic myelomonocytic leukemia 9.7
1009 angioimmunoblastic t-cell lymphoma 9.7
1010 byssinosis 9.7
1011 protein-losing enteropathy 9.7
1012 fanconi syndrome 9.7
1013 open-angle glaucoma 9.7
1014 microcephaly 9.7
1015 ornithosis 9.7
1016 mitral valve insufficiency 9.7
1017 dyscalculia 9.7
1018 nephrocalcinosis 9.7
1019 dementia 9.7
1020 premature ejaculation 9.7
1021 inclusion conjunctivitis 9.7
1022 lymphogranuloma venereum 9.7
1023 root caries 9.7
1024 sporotrichosis 9.7
1025 pneumothorax 9.7
1026 rectum adenocarcinoma 9.7
1027 post-traumatic stress disorder 9.7
1028 dyskeratosis congenita 9.7
1029 hairy cell leukemia 9.7
1030 acute pancreatitis 9.7
1031 iga glomerulonephritis 9.7
1032 wissler-fanconi syndrome 9.7
1033 teratoma 9.7
1034 breast adenocarcinoma 9.7
1035 systemic mastocytosis 9.7
1036 lactic acidosis 9.7
1037 ovary adenocarcinoma 9.7
1038 porokeratosis 9.7
1039 indolent systemic mastocytosis 9.7
1040 mesangial proliferative glomerulonephritis 9.7
1041 movement disease 9.7
1042 agoraphobia 9.7
1043 acute stress disorder 9.7
1044 premenstrual tension 9.7
1045 diverticulitis 9.7
1046 end stage renal disease 9.7
1047 night blindness 9.7
1048 gas gangrene 9.7
1049 achalasia 9.7
1050 pemphigus 9.7
1051 dyskinesia of esophagus 9.7
1052 pompholyx 9.7
1053 exophthalmos 9.7
1054 diabetes insipidus 9.7
1055 keloid disorder 9.7
1056 cluster headache 9.7
1057 dwarfism 9.7
1058 germ cells tumors 9.7
1059 herpes zoster ophthalmicus 9.7
1060 hhv-6 encephalitis 9.7
1061 limbic encephalitis 9.7
1062 polymyositis 9.7
1063 pustular psoriasis 9.7
1064 tuberculous meningitis 9.7
1065 wallerian degeneration 9.7
1066 cerebral atrophy 9.7
1067 hereditary neuropathies 9.7
1068 secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease 9.7
1069 drug-induced vasculitis 9.7
1070 chronic actinic dermatitis 9.7
1071 cancer-associated retinopathy 9.7
1072 pfeiffer syndrome 9.6
1073 caffey disease 9.6
1074 immunoglobulin a deficiency 1 9.6
1075 hand skill, relative 9.6
1076 hypercholesterolemia, familial, 1 9.6
1077 hypertriglyceridemia, familial 9.6
1078 ichthyosis vulgaris 9.6
1079 mastocytosis, cutaneous 9.6
1080 melkersson-rosenthal syndrome 9.6
1081 obsessive-compulsive disorder 9.6
1082 papillomatosis, confluent and reticulated 9.6
1083 scleroderma, familial progressive 9.6
1084 vitiligo-associated multiple autoimmune disease susceptibility 6 9.6
1085 lung cancer 9.6
1086 skin/hair/eye pigmentation, variation in, 2 9.6
1087 anemia, nonspherocytic hemolytic, due to g6pd deficiency 9.6
1088 taqi polymorphism 9.6
1089 yemenite deaf-blind hypopigmentation syndrome 9.6
1090 orthostatic intolerance 9.6
1091 dermatitis, atopic, 3 9.6
1092 dermatitis, atopic, 4 9.6
1093 dermatitis, atopic, 5 9.6
1094 asthma-related traits 2 9.6
1095 hepatitis c virus 9.6
1096 west nile virus 9.6
1097 major affective disorder 8 9.6
1098 major affective disorder 9 9.6
1099 lung cancer susceptibility 3 9.6
1100 asthma-related traits 8 9.6
1101 membranous nephropathy 9.6
1102 striatal degeneration, autosomal dominant 2 9.6
1103 joint laxity, short stature, and myopia 9.6
1104 fetal akinesia deformation sequence 2 9.6
1105 autoimmune pancreatitis 9.6
1106 adenoiditis 9.6
1107 loeys-dietz syndrome 9.6
1108 paralytic poliomyelitis 9.6
1109 autism spectrum disorder 9.6
1110 lymphoma 9.6
1111 fish allergy 9.6
1112 thrombosis 9.6
1113 familial isolated trichomegaly 9.6
1114 dry eye syndrome 9.6
1115 adrenal cortical hypofunction 9.6
1116 pre-eclampsia 9.6
1117 giardiasis 9.6
1118 thrombotic thrombocytopenic purpura 9.6
1119 fiedler's myocarditis 9.6
1120 lipoid nephrosis 9.6
1121 henoch-schoenlein purpura 9.6
1122 anhidrosis 9.6
1123 cercarial dermatitis 9.6
1124 fissured tongue 9.6
1125 myopia 9.6
1126 visual epilepsy 9.6
1127 von willebrand's disease 9.6
1128 brain cancer 9.6
1129 urethritis 9.6
1130 renal tubular acidosis 9.6
1131 cholinergic urticaria 9.6
1132 farmer's lung 9.6
1133 hypothyroidism 9.6
1134 hereditary angioedema 9.6
1135 disease of mental health 9.6
1136 alcohol use disorder 9.6
1137 ichthyosis 9.6
1138 cryptosporidiosis 9.6
1139 vascular disease 9.6
1140 epilepsy 9.6
1141 hepatitis b 9.6
1142 hyperostosis 9.6
1143 ectodermal dysplasia 9.6
1144 thrombocytosis 9.6
1145 polyclonal hypergammaglobulinemia 9.6
1146 neonatal jaundice 9.6
1147 sick building syndrome 9.6
1148 bilirubin metabolic disorder 9.6
1149 tic disorder 9.6
1150 substance abuse 9.6
1151 lipid metabolism disorder 9.6
1152 bipolar disorder 9.6
1153 fibrosarcoma of bone 9.6
1154 plague 9.6
1155 vasomotor rhinitis 9.6
1156 pancreatitis 9.6
1157 thyroid gland disease 9.6
1158 infertility 9.6
1159 complement deficiency 9.6
1160 placenta disease 9.6
1161 cataract 9.6
1162 cyclothymic disorder 9.6
1163 influenza 9.6
1164 seborrheic dermatitis 9.6
1165 amyloidosis 9.6
1166 otitis externa 9.6
1167 polyarteritis nodosa 9.6
1168 refractive error 9.6
1169 hypoglycemia 9.6
1170 47,xyy 9.6
1171 allergic angiitis 9.6
1172 autoimmune encephalitis 9.6
1173 bronchopulmonary dysplasia 9.6
1174 cold urticaria 9.6
1175 dentinogenesis imperfecta type 2 9.6
1176 eosinophilic cystitis 9.6
1177 giant cell myocarditis 9.6
1178 hansen's disease 9.6
1179 lymphomatous thyroiditis 9.6
1180 papular urticaria 9.6
1181 pediatric acute-onset neuropsychiatric syndrome 9.6
1182 prurigo nodularis 9.6
1183 splenomegaly 9.6
1184 depression 9.6
1185 paresthesia 9.6
1186 seizure disorder 9.6
1187 syncope 9.6
1188 cerebrofacial arteriovenous metameric syndrome 9.6
1189 primary cutaneous lymphoma 9.6
1190 idiopathic nephrotic syndrome 9.6
1191 chronic enteropathy associated with slco2a1 gene 9.6
1192 primary eosinophilic gastrointestinal disease 9.6
1193 systemic polyarteritis nodosa 9.6
1194 solar urticaria 9.6
1195 aniridia 1 9.6
1196 carpal tunnel syndrome 9.6
1197 cornea plana 1, autosomal dominant 9.6
1198 vibratory urticaria 9.6
1199 fetal hemoglobin quantitative trait locus 1 9.6
1200 neurofibromatosis, type i 9.6
1201 pernicious anemia 9.6
1202 polykaryocytosis inducer 9.6
1203 actinic prurigo 9.6
1204 porphyria cutanea tarda 9.6
1205 pelvic organ prolapse 9.6
1206 prostate cancer 9.6
1207 pulmonary hypertension, primary, 1 9.6
1208 small cell cancer of the lung 9.6
1209 thrombocytopenic purpura, autoimmune 9.6
1210 williams-beuren syndrome 9.6
1211 afibrinogenemia, congenital 9.6
1212 cornea plana 2, autosomal recessive 9.6
1213 glycogen storage disease ii 9.6
1214 myelofibrosis 9.6
1215 phenylketonuria 9.6
1216 interstitial pneumonitis, desquamative, familial 9.6
1217 reticulum cell sarcoma 9.6
1218 werner syndrome 9.6
1219 kearns-sayre syndrome 9.6
1220 eukaryotic translation elongation factor 1 alpha-1-like 14 9.6
1221 hyperthyroidism, familial gestational 9.6
1222 panbronchiolitis, diffuse 9.6
1223 asthma-related traits 1 9.6
1224 coronary heart disease 1 9.6
1225 mutagen sensitivity 9.6
1226 intraocular pressure quantitative trait locus 9.6
1227 diabetes mellitus, ketosis-prone 9.6
1228 alpha-1-antitrypsin deficiency 9.6
1229 fetal hemoglobin quantitative trait locus 6 9.6
1230 gastric cancer 9.6
1231 barrett esophagus 9.6
1232 leptin deficiency or dysfunction 9.6
1233 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 9.6
1234 leukemia, acute lymphoblastic 3 9.6
1235 hyperprolactinemia 9.6
1236 pachyonychia congenita 3 9.6
1237 tendinopathy 9.6
1238 tendinitis 9.6
1239 aspirin allergy 9.6
1240 chlorhexidine allergy 9.6
1241 restless legs syndrome 9.6
1242 exanthema subitum 9.6
1243 marginal zone b-cell lymphoma 9.6
1244 peripheral t-cell lymphoma 9.6
1245 metabolic acidosis 9.6
1246 hemorrhagic cystitis 9.6
1247 withdrawal disorder 9.6
1248 aphasia 9.6
1249 familial hemiplegic migraine 9.6
1250 scoliosis 9.6
1251 myelomeningocele 9.6
1252 autosomal dominant nocturnal frontal lobe epilepsy 9.6
1253 lymphoproliferative syndrome 9.6
1254 bone resorption disease 9.6
1255 nodal marginal zone lymphoma 9.6
1256 hypogonadotropic hypogonadism 9.6
1257 migraine with aura 9.6
1258 cerebral artery occlusion 9.6
1259 thymus lymphoma 9.6
1260 dermatomyositis 9.6
1261 parotitis 9.6
1262 separation anxiety disorder 9.6
1263 portal hypertension 9.6
1264 primary polycythemia 9.6
1265 methemoglobinemia 9.6
1266 gastric ulcer 9.6
1267 hydrocephalus 9.6
1268 amnestic disorder 9.6
1269 impulse control disorder 9.6
1270 corneal edema 9.6
1271 vitamin k deficiency bleeding 9.6
1272 retinal vasculitis 9.6
1273 prediabetes syndrome 9.6
1274 lyme disease 9.6
1275 spinal muscular atrophy 9.6
1276 pathological gambling 9.6
1277 secondary hyperparathyroidism 9.6
1278 hepatic coma 9.6
1279 hemolytic-uremic syndrome 9.6
1280 ancylostomiasis 9.6
1281 pure red-cell aplasia 9.6
1282 tuberous sclerosis 9.6
1283 hyperparathyroidism 9.6
1284 eclampsia 9.6
1285 patent foramen ovale 9.6
1286 facial paralysis 9.6
1287 adult-onset still's disease 9.6
1288 shoulder impingement syndrome 9.6
1289 neuroleptic malignant syndrome 9.6
1290 glossitis 9.6
1291 chromoblastomycosis 9.6
1292 heart septal defect 9.6
1293 mononeuritis multiplex 9.6
1294 atrial heart septal defect 9.6
1295 endodermal sinus tumor 9.6
1296 leiomyosarcoma 9.6
1297 rectum cancer 9.6
1298 hemorrhagic disease 9.6
1299 transient cerebral ischemia 9.6
1300 hidradenitis 9.6
1301 opiate dependence 9.6
1302 benign mesothelioma 9.6
1303 skin atrophy 9.6
1304 glycogen storage disease 9.6
1305 acalculous cholecystitis 9.6
1306 hemoglobinopathy 9.6
1307 testicular cancer 9.6
1308 grade iii astrocytoma 9.6
1309 early myoclonic encephalopathy 9.6
1310 rhabdomyosarcoma 9.6
1311 temporal lobe epilepsy 9.6
1312 coronary aneurysm 9.6
1313 choriocarcinoma 9.6
1314 aortic aneurysm 9.6
1315 insulinoma 9.6
1316 pancreatic adenocarcinoma 9.6
1317 tick infestation 9.6
1318 coronary stenosis 9.6
1319 hepatitis e 9.6
1320 extracutaneous mastocytoma 9.6
1321 brain edema 9.6
1322 scrapie 9.6
1323 t-cell acute lymphoblastic leukemia 9.6
1324 retinal disease 9.6
1325 hereditary breast ovarian cancer syndrome 9.6
1326 salpingitis 9.6
1327 paraplegia 9.6
1328 transient hypogammaglobulinemia 9.6
1329 cerebrovascular disease 9.6
1330 subacute thyroiditis 9.6
1331 axonal neuropathy 9.6
1332 muscular atrophy 9.6
1333 childhood leukemia 9.6
1334 mite infestation 9.6
1335 viral exanthem 9.6
1336 skin melanoma 9.6
1337 follicular mucinosis 9.6
1338 albinism 9.6
1339 bap1 tumor predisposition syndrome 9.6
1340 malignant hyperthermia susceptibility 9.6
1341 mitochondrial disorders 9.6
1342 airway-centered interstitial fibrosis 9.6
1343 autoimmune enteropathy 9.6
1344 cerulean cataract 9.6
1345 eosinophilic pustular folliculitis 9.6
1346 hemorrhagic proctocolitis 9.6
1347 homologous wasting disease 9.6
1348 leukemia, t-cell, chronic 9.6
1349 mycobacterium fortuitum 9.6
1350 oral cancer 9.6
1351 parainfluenza virus type 3 9.6
1352 pemphigus foliaceus 9.6
1353 pyridoxine deficiency 9.6
1354 soft tissue sarcoma 9.6
1355 sutton disease 2 9.6
1356 aneurysm 9.6
1357 brain injury 9.6
1358 fainting 9.6
1359 hypotonia 9.6
1360 pituitary tumors 9.6
1361 postherpetic neuralgia 9.6
1362 audiogenic seizures 9.6
1363 low-grade astrocytoma 9.6
1364 rare hereditary hemochromatosis 9.6
1365 combined pulmonary fibrosis-emphysema syndrome 9.6
1366 cutaneous pseudolymphoma 9.6
1367 eosinophilic colitis 9.6
1368 argyria 9.6
1369 staphylococcal scarlet fever 9.6
1370 discoid lupus erythematosus 9.6
1371 severe immune-mediated enteropathy 9.6
1372 red cell aplasia 9.6
1373 precursor t-cell acute lymphoblastic leukemia 9.6
1374 aortic aneurysm, familial abdominal, 1 9.5
1375 restless legs syndrome 1 9.5
1376 pseudohypoparathyroidism, type ia 9.5
1377 angelman syndrome 9.5
1378 anisocoria 9.5
1379 arteriovenous malformations of the brain 9.5
1380 progressive familial heart block, type ia 9.5
1381 central core disease of muscle 9.5
1382 chlorpropamide-alcohol flushing 9.5
1383 orofacial cleft 1 9.5
1384 cleft palate, isolated 9.5
1385 major affective disorder 1 9.5
1386 dermal ridges-off-the-end 9.5
1387 erythermalgia, primary 9.5
1388 fucosidase regulator 9.5
1389 gastritis, familial giant hypertrophic 9.5
1390 glioma susceptibility 1 9.5
1391 diaphragmatic hernia, congenital 9.5
1392 hernia, hiatus 9.5
1393 malignant hyperthermia 1 9.5
1394 keloid formation 9.5
1395 keratosis, familial actinic 9.5
1396 leukemia, acute monocytic 9.5
1397 lipomatosis, multiple 9.5
1398 medulloblastoma 9.5
1399 facioscapulohumeral muscular dystrophy 1 9.5
1400 amyotrophy, hereditary neuralgic 9.5
1401 nevus, epidermal 9.5
1402 paroxysmal extreme pain disorder 9.5
1403 benign chronic pemphigus 9.5
1404 phosphatase, acid, of tissues 9.5
1405 pneumothorax, primary spontaneous 9.5
1406 porphyria, acute intermittent 9.5
1407 prader-willi syndrome 9.5
1408 hutchinson-gilford progeria syndrome 9.5
1409 ragweed sensitivity 9.5
1410 raynaud disease 9.5
1411 odontochondrodysplasia 9.5
1412 supravalvular aortic stenosis 9.5
1413 tetralogy of fallot 9.5
1414 thalassemia, beta+, silent allele 9.5
1415 thyroid cancer, nonmedullary, 2 9.5
1416 tobacco addiction 9.5
1417 torticollis 9.5
1418 tuberous sclerosis 1 9.5
1419 urate oxidase, pseudogene 9.5
1420 cardiomyopathy, familial hypertrophic, 1 9.5
1421 zinc finger protein 1 9.5
1422 acrodermatitis enteropathica, zinc-deficiency type 9.5
1423 acromesomelic dysplasia, hunter-thompson type 9.5
1424 acth deficiency, isolated 9.5
1425 albinism, oculocutaneous, type ia 9.5
1426 alopecia universalis congenita 9.5
1427 asthma, nasal polyps, and aspirin intolerance 9.5
1428 australia antigen 9.5
1429 acth-independent macronodular adrenal hyperplasia 9.5
1430 schopf-schulz-passarge syndrome 9.5
1431 ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia 9.5
1432 gastroschisis 9.5
1433 gaucher disease, type i 9.5
1434 monosodium glutamate sensitivity 9.5
1435 multiple acyl-coa dehydrogenase deficiency 9.5
1436 hemolytic uremic syndrome, atypical 1 9.5
1437 hypervitaminosis a 9.5
1438 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 9.5
1439 schimke immunoosseous dysplasia 9.5
1440 lymphoid interstitial pneumonia 9.5
1441 microcephaly 1, primary, autosomal recessive 9.5
1442 mitochondrial complex i deficiency, nuclear type 1 9.5
1443 mucopolysaccharidosis, type vi 9.5
1444 epilepsy, myoclonic juvenile 9.5
1445 netherton syndrome 9.5
1446 insensitivity to pain, congenital, with anhidrosis 9.5
1447 niemann-pick disease, type c1 9.5
1448 3-methylglutaconic aciduria, type iii 9.5
1449 shwachman-diamond syndrome 1 9.5
1450 pierre robin syndrome 9.5
1451 gitelman syndrome 9.5
1452 pulmonary venoocclusive disease 1, autosomal dominant 9.5
1453 rhabdomyosarcoma 2 9.5
1454 rothmund-thomson syndrome, type 2 9.5
1455 testicular germ cell tumor 9.5
1456 thrombocytopenia 3 9.5
1457 usher syndrome, type iia 9.5
1458 kelley-seegmiller syndrome 9.5
1459 hypophosphatemic rickets, x-linked recessive 9.5
1460 sarcoma, synovial 9.5
1461 angioedema induced by ace inhibitors 9.5
1462 wiskott-aldrich syndrome 9.5
1463 arts syndrome 9.5
1464 hemophilia a 9.5
1465 hemophilia b 9.5
1466 glycerol kinase deficiency 9.5
1467 hypophosphatemic rickets, x-linked dominant 9.5
1468 leber optic atrophy 9.5
1469 nuclear ribonucleic acid 9.5
1470 ouabain resistance 9.5
1471 pelizaeus-merzbacher disease 9.5
1472 retinoschisis 1, x-linked, juvenile 9.5
1473 rett syndrome 9.5
1474 spastic paraplegia 2, x-linked 9.5
1475 thrombocytopenia 1 9.5
1476 mitochondrial myopathy, infantile, transient 9.5
1477 myoclonic epilepsy associated with ragged-red fibers 9.5
1478 deafness, aminoglycoside-induced 9.5
1479 exstrophy of bladder 9.5
1480 spinocerebellar ataxia 4 9.5
1481 frontotemporal dementia 9.5
1482 maturity-onset diabetes of the young, type 3 9.5
1483 fryns microphthalmia syndrome 9.5
1484 budd-chiari syndrome 9.5
1485 convulsions, familial infantile, with paroxysmal choreoathetosis 9.5
1486 homocysteinemia 9.5
1487 ventricular fibrillation, paroxysmal familial, 1 9.5
1488 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.5
1489 pars planitis 9.5
1490 aneurysmal bone cysts 9.5
1491 maturity-onset diabetes of the young 9.5
1492 gastrointestinal stromal tumor 9.5
1493 anorexia nervosa 9.5
1494 scheie syndrome 9.5
1495 aortic aneurysm, familial thoracic 1 9.5
1496 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 9.5
1497 bulimia nervosa 9.5
1498 phobia, specific 9.5
1499 legionnaire disease 9.5
1500 lung cancer susceptibility 1 9.5
1501 hyperinsulinemic hypoglycemia, familial, 5 9.5
1502 hyperinsulinemic hypoglycemia, familial, 4 9.5
1503 chilblain lupus 1 9.5
1504 leprosy 4 9.5
1505 smoking as a quantitative trait locus 3 9.5
1506 ewing sarcoma 9.5
1507 sarcoidosis 3 9.5
1508 pseudohypoparathyroidism, type ic 9.5
1509 premature ovarian failure 7 9.5
1510 hearing loss, noise-induced 9.5
1511 nijmegen breakage syndrome-like disorder 9.5
1512 purine nucleoside phosphorylase deficiency 9.5
1513 fatty liver disease, nonalcoholic 1 9.5
1514 hermansky-pudlak syndrome 3 9.5
1515 muscle hypertrophy 9.5
1516 delayed sleep phase disorder 9.5
1517 tumor predisposition syndrome 9.5
1518 cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 9.5
1519 alacrima, achalasia, and mental retardation syndrome 9.5
1520 cholangiocarcinoma 9.5
1521 carbonic anhydrase va deficiency, hyperammonemia due to 9.5
1522 robinow syndrome, autosomal dominant 2 9.5
1523 mental retardation, autosomal dominant 43 9.5
1524 hydrops, lactic acidosis, and sideroblastic anemia 9.5
1525 lung disease, immunodeficiency, and chromosome breakage syndrome 9.5
1526 phenytoin toxicity 9.5
1527 cortical dysplasia, complex, with other brain malformations 10 9.5
1528 silver-russell syndrome 2 9.5
1529 chronic ulcer of skin 9.5
1530 angiosarcoma 9.5
1531 benzylpenicillin allergy 9.5
1532 phenobarbital allergy 9.5
1533 phenytoin allergy 9.5
1534 sulfamethoxazole allergy 9.5
1535 oxirane allergy 9.5
1536 hirata disease 9.5
1537 mineral metabolism disease 9.5
1538 dengue shock syndrome 9.5
1539 subcutaneous mycosis 9.5
1540 acute diarrhea 9.5
1541 lambert-eaton myasthenic syndrome 9.5
1542 penicilliosis 9.5
1543 familial adenomatous polyposis 9.5
1544 usher syndrome 9.5
1545 epidemic typhus 9.5
1546 multinodular goiter 9.5
1547 oculocutaneous albinism 9.5
1548 fetal alcohol syndrome 9.5
1549 spastic cerebral palsy 9.5
1550 fetal alcohol spectrum disorder 9.5
1551 anaplastic large cell lymphoma 9.5
1552 zollinger-ellison syndrome 9.5
1553 first-degree atrioventricular block 9.5
1554 second-degree atrioventricular block 9.5
1555 oculogyric crisis 9.5
1556 colorectal adenocarcinoma 9.5
1557 extra-adrenal pheochromocytoma 9.5
1558 hereditary ataxia 9.5
1559 cd40 ligand deficiency 9.5
1560 ductal carcinoma in situ 9.5
1561 apraxia 9.5
1562 jejunoileitis 9.5
1563 basal ganglia calcification 9.5
1564 uv-sensitive syndrome 9.5
1565 stuttering 9.5
1566 idiopathic scoliosis 9.5
1567 ptosis 9.5
1568 paroxysmal nocturnal hemoglobinuria 9.5
1569 inguinal hernia 9.5
1570 glucocorticoid-induced osteoporosis 9.5
1571 tomato allergy 9.5
1572 erythema elevatum diutinum 9.5
1573 catecholaminergic polymorphic ventricular tachycardia 9.5
1574 primary autosomal recessive microcephaly 9.5
1575 vegetable allergy 9.5
1576 physical disorder 9.5
1577 childhood b-cell acute lymphoblastic leukemia 9.5
1578 cutaneous candidiasis 9.5
1579 hepatic veno-occlusive disease 9.5
1580 superior semicircular canal dehiscence 9.5
1581 non-alcoholic fatty liver disease 9.5
1582 polycystic kidney disease 9.5
1583 familial glucocorticoid deficiency 9.5
1584 aortic dissection 9.5
1585 spinocerebellar ataxia type 1 with axonal neuropathy 9.5
1586 asymptomatic neurosyphilis 9.5
1587 dysplastic nevus syndrome 9.5
1588 cysticercosis 9.5
1589 venous insufficiency 9.5
1590 optic papillitis 9.5
1591 pleomorphic lipoma 9.5
1592 borderline leprosy 9.5
1593 ehrlichiosis 9.5
1594 left bundle branch hemiblock 9.5
1595 asbestosis 9.5
1596 amyotrophic neuralgia 9.5
1597 nasopharyngitis 9.5
1598 orbital granuloma 9.5
1599 osteomalacia 9.5
1600 leukodystrophy 9.5
1601 short bowel syndrome 9.5
1602 frontal sinusitis 9.5
1603 dirofilariasis 9.5
1604 st. louis encephalitis 9.5
1605 cholesteatoma of middle ear 9.5
1606 hemiplegia 9.5
1607 ovarian disease 9.5
1608 depersonalization disorder 9.5
1609 leech infestation 9.5
1610 cholecystolithiasis 9.5
1611 miliaria rubra 9.5
1612 pseudomembranous conjunctivitis 9.5
1613 primary hyperparathyroidism 9.5
1614 orbital cellulitis 9.5
1615 arteriovenous malformation 9.5
1616 retinal microaneurysm 9.5
1617 pneumocystosis 9.5
1618 megacolon 9.5
1619 corneal neovascularization 9.5
1620 epidural abscess 9.5
1621 horner's syndrome 9.5
1622 cardiac tamponade 9.5
1623 diabetic autonomic neuropathy 9.5
1624