Search results for chloride diarrhea

325 hits were found for chloride diarrhea

# Family MCID Name MIFTS Score
1
DRR008 Diarrhea 1, Secretory Chloride, Congenital 47 9.869
2
CNG064 Congenital Chloride Diarrhea 29 7.767
3
P DRR001 Diarrhea 60 0.911
4
CYS001 Cystic Fibrosis 85 0.243
5
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.215
6
P INT068 Intestinal Disease 65 0.215
7
GST050 Gastrointestinal System Disease 66 0.190
8
SCR003 Secretory Diarrhea 36 0.189
9
CLN019 Colonic Disease 55 0.168
10
HYP005 Hypokalemia 53 0.163
11
P KDN018 Kidney Disease 69 0.163
12
CLT003 Colitis 63 0.162
13
DYS015 Dysentery 43 0.159
14
GST045 Gastroenteritis 65 0.158
15
URN009 Urinary System Disease 58 0.153
16
CHL014 Cholera 56 0.139
17
MTB004 Metabolic Acidosis 49 0.138
18
P HPT021 Hepatitis 75 0.138
19
P TRC086 Trichohepatoenteric Syndrome 1 54 0.135
20
AGN016 Aging 65 0.134
21
P PNC044 Pancreatitis 64 0.133
22
LNG099 Lung Disease 67 0.130
23
AST005 Asthma 83 0.122
24
SPS003 Spastic Diplegia 55 0.118
25
P CLR023 Colorectal Cancer 98 0.118
26
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.118
27
DRR016 Diarrhea 2, with Microvillus Atrophy 48 0.117
28
P PNM007 Pneumonia 70 0.114
29
P ART022 Arthritis 77 0.113
30
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 35 0.112
31
ANX010 Anxiety 72 0.109
32
P ENC018 Encephalopathy 58 0.107
33
CRY003 Cryptosporidiosis 51 0.106
34
P INF032 Infertility 59 0.106
35
P ADN016 Adenocarcinoma 71 0.104
36
NRN002 Neuronitis 43 0.104
37
RSP006 Respiratory System Disease 63 0.104
38
OSM001 Osmotic Diarrhea 27 0.103
39
ACQ007 Acquired Immunodeficiency Syndrome 65 0.102
40
P LVR013 Liver Disease 76 0.102
41
P BRS047 Breast Cancer 100 0.101
42
c CNG478 Congenital Diarrhea 23 0.101
43
ADN018 Adenoma 63 0.100
44
P CLC063 Celiac Disease 1 65 0.097
45
CLS016 Clostridium Difficile Colitis 49 0.095
46
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.095
47
P NRP001 Neuropathy 63 0.094
48
P LKM002 Leukemia 75 0.093
49
P DBT009 Diabetes Mellitus 72 0.093
50
CNS004 Constipation 57 0.093
51
MCS002 Mucositis 61 0.092
52
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.092
53
ENT011 Enterocolitis 52 0.090
54
VRL011 Viral Infectious Disease 64 0.090
55
ULC004 Ulcerative Colitis 80 0.090
56
DRM006 Dermatitis 67 0.089
57
PNC034 Pancreas Disease 59 0.087
58
P BRT004 Bartter Disease 52 0.085
59
P ART023 Arthropathy 68 0.082
60
JNT002 Joint Disorders 60 0.082
61
P PRS040 Prostate Cancer 88 0.082
62
P MYP004 Myopathy 69 0.081
63
c CHR089 Chronic Kidney Failure 72 0.080
64
VGN023 Vaginitis 59 0.080
65
P INF037 Inflammatory Bowel Disease 52 0.079
66
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.079
67
P INF038 Influenza 77 0.078
68
P LYM118 Lymphoma 71 0.077
69
CRH001 Crohn's Disease 80 0.077
70
P ANR048 Aniridia 1 68 0.077
71
RCT017 Rectal Disease 38 0.077
72
ANR038 Anorexia Nervosa 1 21 0.077
73
BLD137 Blood Group--Ahonen 17 0.077
74
MNT002 Mental Depression 60 0.075
75
P OST001 Osteopetrosis 70 0.075
76
DDN006 Duodenitis 46 0.074
77
PRT019 Protein-Losing Enteropathy 40 0.074
78
GST053 Gastric Cancer 84 0.072
79
c TRC078 Trichohepatoenteric Syndrome 2 34 0.071
80
NRM005 Neuromuscular Disease 60 0.071
81
STT004 Steatorrhea 41 0.070
82
CMM004 Common Variable Immunodeficiency 71 0.070
83
BRN024 Bronchitis 67 0.069
84
P DBT005 Diabetes Insipidus 54 0.069
85
BRN071 Brain Injury 54 0.068
86
P LNG032 Lung Cancer 99 0.068
87
P HPT023 Hepatocellular Carcinoma 94 0.068
88
P CRV035 Cervical Cancer 72 0.068
89
CNN005 Connective Tissue Disease 65 0.068
90
ALR002 Al-Raqad Syndrome 30 0.067
91
P INT070 Intestinal Obstruction 55 0.067
92
MCN017 Meconium Ileus 52 0.067
93
IRN002 Iron Metabolism Disease 45 0.066
94
HPT082 Hepatic Adenomas, Familial 52 0.065
95
P WSK001 Wiskott-Aldrich Syndrome 76 0.064
96
c INF071 Inflammatory Bowel Disease 1 54 0.064
97
P CTR002 Cataract 60 0.064
98
c BRT052 Bartter Syndrome, Type 1, Antenatal 29 0.064
99
BRS051 Breast Disease 67 0.064
100
c HPT003 Hepatitis a 63 0.063
101
HDC001 Headache 55 0.063
102
VSC011 Vasculitis 66 0.063
103
PRS047 Prostatitis 59 0.063
104
IMM136 Immune System Disease 57 0.063
105
VGN020 Vaginal Disease 44 0.063
106
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 51 0.063
107
CRB009 Cerebritis 41 0.061
108
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.061
109
c HPT001 Hepatitis C 73 0.060
110
LYM042 Lymphocytic Colitis 38 0.060
111
P NRB001 Neuroblastoma 73 0.060
112
DMN002 Dementia 68 0.060
113
P EXN002 Exanthem 62 0.060
114
P CRV039 Cervicitis 49 0.060
115
TRM010 Traumatic Brain Injury 54 0.060
116
HYP267 Hyperchlorhidrosis, Isolated 26 0.060
117
c BRT050 Bartter Syndrome, Type 2, Antenatal 43 0.060
118
ATS010 Autosomal Recessive Disease 40 0.060
119
P MYC084 Mycobacterium Tuberculosis 1 69 0.059
120
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.059
121
CRD223 Cardiac Arrhythmia 52 0.059
122
P RNG031 Ring Chromosome Y Syndrome 29 0.059
123
URT039 Urticaria 59 0.058
124
STM006 Stomach Disease 52 0.058
125
c HPT073 Hepatitis C Virus 73 0.057
126
DYS014 Dyspepsia 54 0.057
127
P SHR001 Short Bowel Syndrome 52 0.057
128
SLP005 Sleep Disorder 59 0.056
129
BCT002 Bacterial Vaginosis 56 0.056
130
PRS042 Prostate Disease 56 0.056
131
P RHM011 Rheumatoid Arthritis 91 0.056
132
BRC012 Brucellosis 71 0.056
133
P HMR005 Hemorrhoid 51 0.056
134
P PSR002 Psoriasis 65 0.055
135
CMM005 Common Cold 62 0.055
136
BRN106 Burns 57 0.055
137
c MTR002 Mitral Valve Insufficiency 46 0.055
138
MYL069 Myeloma, Multiple 86 0.054
139
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.054
140
P CND004 Candidiasis 61 0.054
141
ILT001 Ileitis 52 0.054
142
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.054
143
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.054
144
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 47 0.054
145
P DYS021 Dysautonomia 47 0.054
146
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.054
147
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.054
148
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.054
149
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.054
150
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.054
151
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.054
152
RCT015 Reactive Arthritis 65 0.054
153
HYP056 Hypoglycemia 62 0.054
154
P MTH007 Methemoglobinemia 46 0.054
155
TXC001 Toxic Megacolon 34 0.054
156
LVR012 Liver Cirrhosis 73 0.053
157
BRR014 Barrett Esophagus 64 0.053
158
KRT019 Keratitis, Hereditary 62 0.053
159
P RNL007 Renal Tubular Acidosis 51 0.053
160
SRC014 Sarcoma 68 0.051
161
CHL068 Cholestasis 60 0.051
162
HMT018 Hematopoietic Stem Cell Transplantation 58 0.051
163
P MYS003 Myasthenia Gravis 73 0.051
164
EPD016 Epidermolysis Bullosa 57 0.051
165
c PNS012 Paine Syndrome 52 0.051
166
c BRN108 Branchiootic Syndrome 1 47 0.051
167
DYS073 Dysphagia 47 0.051
168
P CLD001 Cleidocranial Dysplasia 63 0.050
169
P PRP029 Porphyria 62 0.050
170
P HMR003 Hemorrhagic Disease 61 0.050
171
CNT105 Central Core Disease of Muscle 57 0.050
172
ATN005 Autonomic Dysfunction 51 0.050
173
ACT058 Active Peptic Ulcer Disease 43 0.050
174
INT046 Intestinal Tuberculosis 37 0.050
175
LPS020 Lipase Deficiency, Combined 31 0.050
176
AMY010 Amyloidosis Beta2m 14 0.050
177
STR067 Stroke, Ischemic 84 0.049
178
BRN022 Bronchiectasis 55 0.049
179
HDN002 Head Injury 48 0.049
180
P RNL045 Renal Tubular Acidosis, Distal 42 0.049
181
SVR066 Severe Combined Immunodeficiency, X-Linked 63 0.047
182
SCH014 Schistosomiasis 62 0.047
183
c PSD112 Pseudohypoaldosteronism, Type I, Autosomal Dominant 45 0.047
184
ESP018 Esophageal Candidiasis 44 0.047
185
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.047
186
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.047
187
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.045
188
P CNJ013 Conjunctivitis 67 0.045
189
P KDN017 Kidney Cancer 66 0.045
190
HYP066 Hyperglycemia 64 0.045
191
P NPH012 Nephrotic Syndrome 60 0.045
192
P LRY019 Laryngitis 57 0.045
193
P HYP726 Hypercalcemia, Infantile, 1 57 0.045
194
P HYP076 Hyperthyroidism 56 0.045
195
P THY032 Thyroiditis 56 0.045
196
CRV040 Cervix Carcinoma 52 0.045
197
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 40 0.045
198
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.045
199
DYS011 Dyskinesia of Esophagus 39 0.045
200
LRY017 Laryngeal Disease 38 0.045
201
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 36 0.045
202
PHT004 Photoallergic Dermatitis 25 0.045
203
MTH075 Methionine Malabsorption Syndrome 16 0.045
204
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.044
205
P OVR042 Ovarian Cancer 82 0.044
206
ALL003 Allergic Rhinitis 68 0.044
207
GST092 Gastroesophageal Reflux 64 0.044
208
P MRC003 Mercury Poisoning 50 0.044
209
NRR001 Neuroretinitis 46 0.044
210
P BLD051 Blood Coagulation Disease 38 0.044
211
SWL001 Swallowing Disorders 36 0.044
212
P PNC035 Pancreatic Cancer 89 0.043
213
CRB037 Cerebral Palsy 70 0.043
214
P BCL006 B-Cell Lymphomas 70 0.043
215
PRT036 Peritonitis 67 0.043
216
MXD005 Mixed Connective Tissue Disease 66 0.043
217
P THR014 Thrombocytopenia 65 0.043
218
c ATM011 Autoimmune Hepatitis 63 0.043
219
RCK004 Rickets 63 0.043
220
P GRV001 Graves' Disease 62 0.043
221
P TCL004 T-Cell Leukemia 50 0.043
222
ERY029 Erythermalgia, Primary 48 0.043
223
MRG013 Mirage Syndrome 44 0.043
224
P CRB059 Cerebellar Degeneration 40 0.043
225
DDN007 Duodenal Disease 38 0.043
226
PNM003 Pneumatosis Cystoides Intestinalis 31 0.043
227
FNC006 Functional Gastric Disease 26 0.043
228
GST004 Gastric Neuroendocrine Neoplasm 25 0.043
229
c GST091 Gastrointestinal Neuroendocrine Benign Tumor 21 0.043
230
SCK003 Sickle Cell Anemia 73 0.039
231
GLL018 Gallbladder Cancer 67 0.039
232
P HYP086 Hypothyroidism 62 0.039
233
ESP023 Esophageal Disease 58 0.039
234
PND002 Pendred Syndrome 55 0.039
235
P SCL009 Sclerosing Cholangitis 53 0.039
236
ATN002 Autonomic Nervous System Disease 51 0.039
237
DNT012 Dental Caries 50 0.039
238
PST011 Pustulosis of Palm and Sole 47 0.039
239
NTR005 Nutritional Deficiency Disease 46 0.039
240
CRN019 Coronary Artery Vasospasm 42 0.039
241
FXF002 Fox-Fordyce Disease 40 0.039
242
VSC008 Vascular Hemostatic Disease 36 0.039
243
c MYS011 Myasthenia Gravis Congenital 28 0.039
244
P AST055 Asthma-Related Traits 1 18 0.039
245
P DLT002 Dilated Cardiomyopathy 76 0.038
246
c MLT160 Multiple Endocrine Neoplasia, Type Iia 65 0.038
247
P HYP040 Hypospadias 60 0.038
248
GNR004 Generalized Anxiety Disorder 53 0.038
249
STM007 Stomatitis 52 0.038
250
c GRV008 Graves Disease 1 52 0.038
251
PRP007 Priapism 49 0.038
252
ASP007 Aspiration Pneumonia 49 0.038
253
EWN002 Ewing's Family of Tumors 49 0.038
254
ESP002 Esophageal Varix 46 0.038
255
ATN004 Autonomic Neuropathy 46 0.038
256
ASP008 Aspiration Pneumonitis 45 0.038
257
HYP017 Hypophosphatemia 45 0.038
258
MYP100 Myopathy, X-Linked, with Excessive Autophagy 44 0.038
259
HRN026 Hernia, Hiatus 42 0.038
260
SPR007 Superior Mesenteric Artery Syndrome 42 0.038
261
CNG436 Congenital Disorder of Deglycosylation 40 0.038
262
HPT004 Hepatic Coma 40 0.038
263
PPT001 Peptic Esophagitis 40 0.038
264
RMN001 Rumination Disorder 39 0.038
265
CPL005 Capillary Disease 38 0.038
266
LTR003 Lateral Medullary Syndrome 38 0.038
267
GST020 Gastric Antral Vascular Ectasia 37 0.038
268
PRS063 Paresthesia 36 0.038
269
BLR002 Bile Reflux 34 0.038
270
LRY007 Laryngeal Tuberculosis 33 0.038
271
c ACT072 Acute Laryngitis 33 0.038
272
ESP029 Esophageal Atresia/tracheoesophageal Fistula 32 0.038
273
NNT005 Neonatal Candidiasis 32 0.038
274
PNC028 Pancreatic Steatorrhea 31 0.038
275
BLD041 Bladder Calculus 30 0.038
276
ANS018 Anismus 29 0.038
277
CHR067 Chronic Intestinal Vascular Insufficiency 29 0.038
278
GRN011 Granulomatous Gastritis 28 0.038
279
GST090 Gastroduodenal Crohn's Disease 28 0.038
280
P STR035 Streptococcal Group a Invasive Disease 28 0.038
281
PST014 Postsurgical Hypothyroidism 28 0.038
282
ISC001 Ischemic Neuropathy 26 0.038
283
SQM005 Squamous Papillomatosis 23 0.038
284
HRY002 Hairy Tongue 22 0.038
285
LWR004 Lower Urinary Tract Calculus 22 0.038
286
BLC017 Black Hairy Tongue 19 0.038
287
FNG003 Fungal Esophagitis 19 0.038
288
RNL111 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia 18 0.038
289
P LNG064 Lung Cancer Susceptibility 3 64 0.032
290
BRG013 Buerger Disease 62 0.032
291
DBT010 Diabetic Neuropathy 60 0.032
292
P MLT074 Multiple Endocrine Neoplasia 55 0.032
293
DST005 Diastrophic Dysplasia 54 0.032
294
ADR013 Adrenal Gland Hyperfunction 54 0.032
295
SPN041 Spinal Cord Disease 54 0.032
296
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.032
297
P OBS001 Obstructive Jaundice 53 0.032
298
CLN015 Colon Adenocarcinoma 53 0.032
299
P PNV001 Panuveitis 52 0.032
300
PLR008 Pleurisy 52 0.032
301
THY030 Thyroid Gland Disease 51 0.032
302
PLS009 Plasma Cell Neoplasm 51 0.032
303
SKL017 Skeletal Dysplasias 48 0.032
304
c ACT078 Acute Porphyria 48 0.032
305
PLY012 Polyhydramnios 47 0.032
306
c ACH042 Achondrogenesis, Type Ib 46 0.032
307
PRD003 Periodontosis 45 0.032
308
EXC002 Exocrine Pancreatic Insufficiency 45 0.032
309
ESN004 Eosinophilic Gastritis 44 0.032
310
c CHR020 Chronic Interstitial Cystitis 44 0.032
311
ESP025 Esophagus Adenocarcinoma 42 0.032
312
SPN369 Spinal Disease 42 0.032
313
LCH004 Lichen Disease 42 0.032
314
c SCN052 Secondary Adrenal Insufficiency 41 0.032
315
c DFN354 Deafness, Autosomal Dominant 20 40 0.032
316
P BRN120 Bronchus Cancer 39 0.032
317
PRL008 Paralytic Ileus 38 0.032
318
CLC011 Cloacal Exstrophy 38 0.032
319
PPT002 Peptic Ulcer Perforation 38 0.032
320
c DFN124 Deafness, Autosomal Recessive 6 38 0.032
321
c CHR057 Chronic Laryngitis 34 0.032
322
VLV036 Vulvar Disease 33 0.032
323
PNC012 Punctate Epithelial Keratoconjunctivitis 29 0.032
324
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.032
325
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.032
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