Search results for "malnutrition"

The MalaCard for "malnutrition" has been retired.
Searching MalaCards for entries containing "malnutrition"

478 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 49 7.300
2
NTR005 Nutritional Deficiency Disease 36 3.319
3
KWS001 Kwashiorkor 40 0.202
4
P DRR001 Diarrhea 60 0.182
5
MRS001 Marasmus 36 0.146
6
MLR004 Malaria 83 0.139
7
PRT036 Peritonitis 63 0.139
8
P HPT021 Hepatitis 69 0.132
9
c ACT004 Acute Diarrhea 39 0.132
10
P PNC044 Pancreatitis 61 0.118
11
ACD009 Acid-Labile Subunit, Deficiency of 45 0.110
12
P OBS005 Obesity 92 0.105
13
ETN001 Eating Disorder 58 0.105
14
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.101
15
ATH003 Atherosclerosis 65 0.101
16
XRP001 Xerophthalmia 33 0.101
17
c DRR009 Diarrhea 6 29 0.101
18
INS024 Insulin-Like Growth Factor I 75 0.096
19
LVR012 Liver Cirrhosis 67 0.096
20
DFC004 Deficiency Anemia 64 0.096
21
P ANR007 Anorexia Nervosa 61 0.096
22
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.096
23
P PNM007 Pneumonia 68 0.091
24
P THY032 Thyroiditis 54 0.091
25
P INF038 Influenza 72 0.086
26
P KDN018 Kidney Disease 66 0.086
27
P RCK004 Rickets 61 0.086
28
MSL001 Measles 61 0.086
29
LPD004 Lipoid Nephrosis 48 0.086
30
ASC002 Ascariasis 39 0.086
31
MSC004 Muscle Tissue Disease 34 0.086
32
CYS001 Cystic Fibrosis 83 0.080
33
P LVR013 Liver Disease 75 0.080
34
ISC004 Ischemia 61 0.080
35
ALC006 Alcoholic Hepatitis 59 0.080
36
URM002 Uremia 48 0.080
37
GRD001 Giardiasis 40 0.080
38
P LKM002 Leukemia 71 0.074
39
TBR010 Tuberculosis 70 0.074
40
c CHR089 Chronic Kidney Failure 66 0.074
41
ADM013 Adamantinoma of Long Bones 57 0.074
42
KRT002 Keratomalacia 52 0.074
43
IRN001 Iron Deficiency Anemia 52 0.074
44
P PLL002 Pellagra 45 0.074
45
BNS002 Bone Structure Disease 37 0.074
46
TRP004 Tropical Sprue 35 0.074
47
P CLR023 Colorectal Cancer 97 0.068
48
P ART022 Arthritis 75 0.068
49
CNG034 Congestive Heart Failure 72 0.068
50
MRB003 Morbid Obesity 59 0.068
51
END030 End Stage Renal Failure 55 0.068
52
FDL002 Food Allergy 53 0.068
53
MTB004 Metabolic Acidosis 48 0.068
54
P NGH001 Night Blindness 48 0.068
55
DYS073 Dysphagia 48 0.068
56
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.068
57
PRT019 Protein-Losing Enteropathy 42 0.068
58
SPC010 Speech and Communication Disorders 41 0.068
59
CRB009 Cerebritis 39 0.068
60
c DRR007 Diarrhea 7 31 0.068
61
P RHM011 Rheumatoid Arthritis 89 0.061
62
c HPT001 Hepatitis C 68 0.061
63
P MNN013 Meningitis 67 0.061
64
P OST002 Osteoporosis 64 0.061
65
P INT068 Intestinal Disease 60 0.061
66
P GST049 Gastrointestinal System Cancer 60 0.061
67
c ACT073 Acute Leukemia 60 0.061
68
WLM001 Wolman Disease 57 0.061
69
CHY002 Chylomicron Retention Disease 57 0.061
70
CLN019 Colonic Disease 51 0.061
71
OVR063 Overnutrition 50 0.061
72
LRN003 Learning Disability 49 0.061
73
c HMG001 Hemoglobin C Disease 47 0.061
74
INT253 Intestinal Benign Neoplasm 47 0.061
75
CRY003 Cryptosporidiosis 46 0.061
76
LCT002 Lactose Intolerance 46 0.061
77
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.061
78
BRN080 Brain Ischemia 41 0.061
79
BLD054 Blood Protein Disease 37 0.061
80
IMP003 Impaired Renal Function Disease 34 0.061
81
c HMG004 Hemoglobin D Disease 31 0.061
82
BNM008 Bone Mineral Density, Low 16 0.061
83
P HPT023 Hepatocellular Carcinoma 92 0.053
84
P PNC035 Pancreatic Cancer 87 0.053
85
P HRT032 Heart Disease 75 0.053
86
CRH001 Crohn's Disease 75 0.053
87
P NRB001 Neuroblastoma 70 0.053
88
P CRD011 Cardiomyopathy 68 0.053
89
P CLC005 Celiac Disease 68 0.053
90
P MYP004 Myopathy 67 0.053
91
LSH001 Leishmaniasis 66 0.053
92
P INF037 Inflammatory Bowel Disease 63 0.053
93
P ESP024 Esophagitis 61 0.053
94
ACQ007 Acquired Immunodeficiency Syndrome 60 0.053
95
c VRL010 Viral Hepatitis 60 0.053
96
WLL006 Wells Syndrome 59 0.053
97
P HYP060 Hyperinsulinism 58 0.053
98
PNC034 Pancreas Disease 58 0.053
99
CHL071 Child Syndrome 58 0.053
100
VSC003 Visceral Leishmaniasis 56 0.053
101
MCS002 Mucositis 55 0.053
102
RCT018 Rectal Neoplasm 54 0.053
103
KDS001 Kid Syndrome 53 0.053
104
BRN106 Burns 52 0.053
105
P SPS003 Spastic Diplegia 52 0.053
106
BRN071 Brain Injury 52 0.053
107
VSC044 Visceral Myopathy 51 0.053
108
STM006 Stomach Disease 50 0.053
109
BNF002 Bone Fracture 50 0.053
110
P MSC003 Muscular Atrophy 50 0.053
111
URN009 Urinary System Disease 50 0.053
112
CSY001 C Syndrome 50 0.053
113
HYP037 Hyperhomocysteinemia 50 0.053
114
P URF003 Urofacial Syndrome 1 50 0.053
115
SCR002 Scurvy 46 0.053
116
ALN001 Aland Island Eye Disease 45 0.053
117
GDS001 Good Syndrome 44 0.053
118
ANC001 Ancylostomiasis 44 0.053
119
c HMG003 Hemoglobin E Disease 44 0.053
120
SXL003 Sexual Disorder 42 0.053
121
BRB001 Beriberi 41 0.053
122
PRS036 Parasitic Protozoa Infectious Disease 41 0.053
123
DYS015 Dysentery 40 0.053
124
PSD029 Pseudocholinesterase Deficiency 40 0.053
125
RCT017 Rectal Disease 40 0.053
126
ADJ001 Adjustment Disorder 38 0.053
127
c PNC106 Pancreatic Agenesis 1 37 0.053
128
FNC002 Functional Diarrhea 37 0.053
129
BTN004 Biotin Deficiency 34 0.053
130
CHR028 Chronic Wasting Disease 34 0.053
131
PLC008 Placenta Disease 33 0.053
132
ADS015 Aids Wasting Syndrome 17 0.053
133
P LNG032 Lung Cancer 95 0.043
134
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.043
135
P SCH015 Schizophrenia 77 0.043
136
c DLT002 Dilated Cardiomyopathy 76 0.043
137
P NRV007 Nervous System Disease 71 0.043
138
P RSP003 Respiratory Failure 71 0.043
139
c HPT016 Hepatitis B 65 0.043
140
P LYM026 Lymphoblastic Leukemia 62 0.043
141
MTH009 Mouth Disease 61 0.043
142
TTN003 Tetanus 61 0.043
143
P NRP001 Neuropathy 59 0.043
144
LPD008 Lipid Metabolism Disorder 58 0.043
145
RSP006 Respiratory System Disease 58 0.043
146
P CTR002 Cataract 58 0.043
147
P MCR010 Microcephaly 58 0.043
148
SCH014 Schistosomiasis 58 0.043
149
c PRC016 Pre-Eclampsia 56 0.043
150
GST050 Gastrointestinal System Disease 56 0.043
151
VRL011 Viral Infectious Disease 55 0.043
152
c BCT007 Bacterial Meningitis 54 0.043
153
GST037 Gastroparesis 54 0.043
154
NTH001 Netherton Syndrome 54 0.043
155
DSS008 Disease of Mental Health 52 0.043
156
GTR002 Goiter 52 0.043
157
ALL026 Allergic Hypersensitivity Disease 52 0.043
158
P MSC033 Muscle Disorders 52 0.043
159
P PRC031 Preeclampsia/eclampsia 1 51 0.043
160
PRC012 Pericardial Effusion 51 0.043
161
MCR094 Microvillus Inclusion Disease 50 0.043
162
END035 Endocrine Gland Cancer 49 0.043
163
P SHR001 Short Bowel Syndrome 49 0.043
164
ALC009 Alcoholic Liver Cirrhosis 49 0.043
165
MSS002 Mass Syndrome 48 0.043
166
CRD002 Cri-Du-Chat Syndrome 48 0.043
167
PRT030 Parathyroid Gland Disease 47 0.043
168
GST009 Gastroschisis 47 0.043
169
TBR011 Tuberculous Meningitis 47 0.043
170
DNT012 Dental Caries 46 0.043
171
RLP003 Relapsing Fever 45 0.043
172
c CLR085 Colorectal Cancer 1 45 0.043
173
BWN001 Bowen-Conradi Syndrome 44 0.043
174
AMB001 Amebiasis 43 0.043
175
EXC002 Exocrine Pancreatic Insufficiency 43 0.043
176
P CRB088 Cerebral Atrophy 43 0.043
177
TRC023 Trichinosis 42 0.043
178
AYM001 Ayme-Gripp Syndrome 41 0.043
179
ANM001 Anemia of Prematurity 41 0.043
180
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.043
181
END038 Endocrine Pancreas Disease 41 0.043
182
DNT001 Dental Fluorosis 41 0.043
183
FTL021 Fetal Macrosomia 41 0.043
184
ATX003 Ataxia with Isolated Vitamin E Deficiency 40 0.043
185
c HYP058 Hypervitaminosis a 39 0.043
186
NCR001 Necrotizing Ulcerative Gingivitis 38 0.043
187
c CNG413 Congenital Short Bowel Syndrome 36 0.043
188
ALR002 Al-Raqad Syndrome 36 0.043
189
NNT011 Neonatal Anemia 33 0.043
190
HNS001 Hansen's Disease 30 0.043
191
VTM003 Vitamin Metabolic Disorder 30 0.043
192
c PNC111 Pancreatic Cancer 2 28 0.043
193
c PNC094 Pancreatic Cancer 1 27 0.043
194
P INT103 Intrauterine Infections 22 0.043
195
c CRN214 Coronary Heart Disease 5 22 0.043
196
NDD001 Nodding Syndrome 18 0.043
197
ATR076 Atrophic Muscular Disease 15 0.043
198
c DLT001 Delta Chain Disease 13 0.043
199
c SYS001 Systemic Lupus Erythematosus 86 0.030
200
HV1006 Hiv-1 80 0.030
201
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.030
202
DCH001 Duchenne Muscular Dystrophy 79 0.030
203
GST053 Gastric Cancer 78 0.030
204
P HYP607 Hypercholesterolemia, Familial 76 0.030
205
STR067 Stroke, Ischemic 75 0.030
206
P CRN211 Coronary Artery Disease 74 0.030
207
c HPT073 Hepatitis C Virus 73 0.030
208
P HMC003 Hemochromatosis 72 0.030
209
SCK003 Sickle Cell Anemia 71 0.030
210
SQM006 Squamous Cell Carcinoma 70 0.030
211
BCK001 Becker Muscular Dystrophy 69 0.030
212
P LYM118 Lymphoma 69 0.030
213
c HYP595 Hypertension, Essential 69 0.030
214
PRP027 Peripheral Vascular Disease 69 0.030
215
ISC006 Ischemic Heart Disease 68 0.030
216
PCK002 Pick Disease 68 0.030
217
PLM001 Pulmonary Tuberculosis 67 0.030
218
CHG001 Chagas Disease 67 0.030
219
VSC007 Vascular Disease 67 0.030
220
SKN016 Skin Disease 66 0.030
221
OBS002 Obsessive-Compulsive Disorder 66 0.030
222
P MSC005 Muscular Dystrophy 65 0.030
223
P TRN020 Turner Syndrome 65 0.030
224
P KDN017 Kidney Cancer 65 0.030
225
DMN002 Dementia 65 0.030
226
P AMY004 Amyloidosis 65 0.030
227
P LPS004 Lupus Erythematosus 64 0.030
228
P THL005 Thalassemia 64 0.030
229
CHD001 Chediak-Higashi Syndrome 64 0.030
230
P PRM019 Premature Ovarian Failure 64 0.030
231
LNG099 Lung Disease 64 0.030
232
WLM007 Wilms Tumor Susceptibility-5 63 0.030
233
P PRD008 Periodontitis 63 0.030
234
CRB039 Cerebrovascular Disease 63 0.030
235
P CRD013 Cardiofaciocutaneous Syndrome 63 0.030
236
P ENC004 Encephalitis 63 0.030
237
P PRT010 Parathyroid Carcinoma 63 0.030
238
BLM001 Bloom Syndrome 63 0.030
239
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.030
240
c ATS347 Autosomal Dominant Polycystic Kidney Disease 63 0.030
241
GNG013 Gingivitis 61 0.030
242
HYP056 Hypoglycemia 61 0.030
243
HYP066 Hyperglycemia 61 0.030
244
OVR029 Ovarian Hyperstimulation Syndrome 61 0.030
245
APP008 Appendicitis 60 0.030
246
PRM097 Primary Immunodeficiency Disease 60 0.030
247
RBR001 Roberts Syndrome 60 0.030
248
P ORL007 Oral Cavity Cancer 59 0.030
249
c HPT003 Hepatitis a 59 0.030
250
GST045 Gastroenteritis 59 0.030
251
P ENC018 Encephalopathy 59 0.030
252
STT001 Status Epilepticus 59 0.030
253
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 59 0.030
254
P ALC004 Alcohol Abuse 59 0.030
255
ART021 Arteriosclerosis 58 0.030
256
P CMR001 Camurati-Engelmann Disease 58 0.030
257
IRR002 Irritable Bowel Syndrome 58 0.030
258
P HYP069 Hyperparathyroidism 58 0.030
259
BNC003 Bone Cancer 58 0.030
260
P HRS035 Hirschsprung Disease 1 58 0.030
261
P CND004 Candidiasis 57 0.030
262
CTS003 Coats Disease 57 0.030
263
P EXN002 Exanthem 57 0.030
264
ORL011 Oral Cancer 56 0.030
265
NRM005 Neuromuscular Disease 56 0.030
266
ZLL001 Zellweger Syndrome 56 0.030
267
HYP266 Hypoxia 56 0.030
268
c HYP615 Hyperparathyroidism, Familial Primary 56 0.030
269
c HRD002 Hereditary Angioedema 55 0.030
270
c MSC124 Muscular Dystrophy, Congenital 55 0.030
271
GLC003 Glucose Intolerance 55 0.030
272
P LPD010 Lipodystrophy 55 0.030
273
P HYP076 Hyperthyroidism 55 0.030
274
CLF027 Cleft Palate, Isolated 55 0.030
275
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.030
276
PLS007 Plasmodium Falciparum Malaria 55 0.030
277
P HRD011 Hereditary Spherocytosis 54 0.030
278
P HYP083 Hypopituitarism 54 0.030
279
c PND001 Pain Disorder 54 0.030
280
c VRL007 Viral Encephalitis 54 0.030
281
SHG001 Shigellosis 54 0.030
282
CND002 Conduct Disorder 54 0.030
283
P ECL001 Eclampsia 54 0.030
284
CYS005 Cysticercosis 54 0.030
285
C3D001 C3 Deficiency 53 0.030
286
P PLY014 Polycystic Kidney Disease 53 0.030
287
P FTL001 Fetal Alcohol Syndrome 53 0.030
288
PLS006 Plasmodium Vivax Malaria 53 0.030
289
P DGR001 Digeorge Syndrome 53 0.030
290
CHL014 Cholera 53 0.030
291
MNT002 Mental Depression 53 0.030
292
ACH005 Achalasia 52 0.030
293
ADL002 Adult Syndrome 52 0.030
294
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.030
295
P FRC002 Fructose Intolerance 52 0.030
296
OCL008 Oculopharyngeal Muscular Dystrophy 52 0.030
297
P ANG015 Angioedema 52 0.030
298
c HPT015 Hepatitis D 52 0.030
299
P PNC001 Pancytopenia 52 0.030
300
BCT002 Bacterial Vaginosis 52 0.030
301
SLM003 Salmonellosis 52 0.030
302
PRT011 Protein C Deficiency 52 0.030
303
LYS003 Lysinuric Protein Intolerance 52 0.030
304
MYC002 Mycobacterium Avium Complex Disease 52 0.030
305
URC002 Urea Cycle Disorder 51 0.030
306
DBT062 Diabetic Foot Ulcers 51 0.030
307
P GND004 Gonadal Dysgenesis 51 0.030
308
IMM136 Immune System Disease 51 0.030
309
P PRC019 Precocious Puberty 51 0.030
310
VND002 Van Der Woude Syndrome 50 0.030
311
GRW007 Growth Hormone Deficiency 50 0.030
312
RTN023 Retinitis 50 0.030
313
P CHR345 Chronic Pain 50 0.030
314
PRL032 Perlman Syndrome 50 0.030
315
HPT074 Hepatic Adenoma, Somatic 50 0.030
316
PLC005 Placental Insufficiency 50 0.030
317
ONC002 Onchocerciasis 49 0.030
318
MSC072 Muscle Cancer 49 0.030
319
c CNT075 Central Precocious Puberty 49 0.030
320
WHP001 Whipple Disease 49 0.030
321
BLR007 Biliary Tract Neoplasm 49 0.030
322
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.030
323
P FML035 Familial Hyperlipidemia 48 0.030
324
OBS001 Obstructive Jaundice 48 0.030
325
THL018 Thalassemia Major 48 0.030
326
P TRC086 Trichohepatoenteric Syndrome 1 48 0.030
327
P RNL015 Renal Hypertension 48 0.030
328
VND001 Vein Disease 47 0.030
329
MLK006 Milk Allergy 47 0.030
330
P TCL004 T-Cell Leukemia 47 0.030
331
DWR001 Dwarfism 47 0.030
332
SCB001 Scabies 47 0.030
333
TRC008 Trachoma 47 0.030
334
HMS001 Hemosiderosis 46 0.030
335
CRB025 Carbohydrate Metabolic Disorder 46 0.030
336
c INT072 Intestinal Pseudo-Obstruction 46 0.030
337
GLT021 Glutaricaciduria, Type I 46 0.030
338
INC022 Inclusion-Cell Disease 46 0.030
339
MGC001 Megacolon 45 0.030
340
CRB004 Cerebral Artery Occlusion 45 0.030
341
ACR041 Acromelic Frontonasal Dysostosis 45 0.030
342
TCL003 T Cell Deficiency 45 0.030
343
BCT004 Bacteriuria 45 0.030
344
HDN002 Head Injury 45 0.030
345
CCN007 Cocoon Syndrome 45 0.030
346
P ANL018 Analbuminemia 44 0.030
347
P SDR002 Siderosis 44 0.030
348
HYP085 Hypothalamic Disease 44 0.030
349
CRD118 Cardiovascular Cancer 44 0.030
350
GLS007 Glossitis 44 0.030
351
SKN023 Skin Tag 44 0.030
352
HYP077 Hypertrichosis 44 0.030
353
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.030
354
CRR007 Cirrhosis, Cryptogenic 43 0.030
355
PHY002 Physical Disorder 43 0.030
356
BRT030 Birth Defects 43 0.030
357
RNL097 Renal Artery Disease 43 0.030
358
SKN027 Skin Conditions 43 0.030
359
LKC003 Leukocyte Disease 43 0.030
360
WRN003 Wernicke Encephalopathy 43 0.030
361
HYP081 Hypolipoproteinemia 42 0.030
362
END072 Endotheliitis 42 0.030
363
NM001 Noma 42 0.030
364
IMP004 Impetigo 42 0.030
365
GLC008 Glucose Metabolism Disease 42 0.030
366
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.030
367
MCR017 Macrocytic Anemia 42 0.030
368
SPR007 Superior Mesenteric Artery Syndrome 41 0.030
369
IRN002 Iron Metabolism Disease 41 0.030
370
P HVY001 Heavy Chain Disease 41 0.030
371
PRM025 Primary Bacterial Infectious Disease 41 0.030
372
VGN020 Vaginal Disease 41 0.030
373
RPR002 Reproductive System Disease 41 0.030
374
CNT025 Central Pontine Myelinolysis 41 0.030
375
TNS007 Taeniasis 41 0.030
376
AMN006 Aminoaciduria 41 0.030
377
c PRG106 Progressive Muscular Dystrophy 40 0.030
378
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.030
379
STT004 Steatorrhea 40 0.030
380
c PRM212 Primary Microcephaly 40 0.030
381
ADT003 Auditory System Disease 40 0.030
382
c CHR096 Chronic Pulmonary Heart Disease 40 0.030
383
PYM001 Pyomyositis 40 0.030
384
MCR020 Microsporidiosis 39 0.030
385
MNR003 Mineral Metabolism Disease 38 0.030
386
ALC010 Alcoholic Cardiomyopathy 38 0.030
387
P FML187 Familial Hypertension 38 0.030
388
SCN001 Secondary Hyperparathyroidism of Renal Origin 38 0.030
389
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.030
390
TRC077 Trichomegaly 38 0.030
391
SPC003 Specific Developmental Disorder 38 0.030
392
P RTN022 Retinal Vein Occlusion 38 0.030
393
C1N001 C1 Inhibitor Deficiency 38 0.030
394
SNL007 Senile Cataract 37 0.030
395
PRP080 Peripheral Artery Disease 37 0.030
396
GNR003 Generalized Atherosclerosis 37 0.030
397
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.030
398
NSY001 N Syndrome 36 0.030
399
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.030
400
ANR018 Anorchia 36 0.030
401
SPL040 Split Hand 36 0.030
402
SML020 Small Patella Syndrome 36 0.030
403
PYR016 Pyridoxine Deficiency 36 0.030
404
c CNT016 Central Retinal Vein Occlusion 36 0.030
405
ACR005 Acrodermatitis 36 0.030
406
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.030
407
PRT035 Peritoneum Cancer 35 0.030
408
ASP004 Asphyxia Neonatorum 35 0.030
409
ECT004 Ecthyma 35 0.030
410
FLC001 Folic Acid Deficiency Anemia 34 0.030
411
RMN001 Rumination Disorder 34 0.030
412
MTC061 Mitochondrial Dna Depletion Syndrome 1 34 0.030
413
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 0.030
414
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.030
415
c HYP311 Hyperparathyroidism 3 33 0.030
416
RFR013 Refractory Celiac Disease 33 0.030
417
ACD004 Acdc 33 0.030
418
c CRD187 Cardiomyopathy, Dilated, 3b 33 0.030
419
DDN007 Duodenal Disease 33 0.030
420
FNC006 Functional Gastric Disease 32 0.030
421
ANS012 Anus Disease 32 0.030
422
SKL007 Skeletal Muscle Regeneration 32 0.030
423
PYR004 Pyuria 32 0.030
424
CHY005 Chylothorax, Congenital 30 0.030
425
BRL001 Brill-Zinsser Disease 30 0.030
426
ATR073 Atrophic Glossitis 30 0.030
427
IMM068 Immunodeficiency 8 30 0.030
428
WHT017 Wheat Allergy 30 0.030
429
TMP011 Temple-Baraitser Syndrome 30 0.030
430
c CNT068 Central Pain Syndrome 29 0.030
431
MRG013 Mirage Syndrome 29 0.030
432
IDP034 Idiopathic Central Precocious Puberty 29 0.030
433
PRM243 Primary Bone Cancer 29 0.030
434
FSH003 Fish Allergy 29 0.030
435
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 28 0.030
436
c HMG029 Hemoglobin Se Disease 28 0.030
437
OSM001 Osmotic Diarrhea 28 0.030
438
P KLZ004 Kala-Azar 1 28 0.030
439
OST097 Osteoporotic Fracture 28 0.030
440
CRB031 Cerebral Arterial Disease 27 0.030
441
c INF002 Inflammatory Diarrhea 27 0.030
442
c PRC047 Precocious Puberty, Central, 1 26 0.030
443
SCR037 Sucrase-Isomaltase Deficiency, Congenital 26 0.030
444
c ANR038 Anorexia Nervosa 1 26 0.030
445
P PLT008 Pili Torti 25 0.030
446
c ADL096 Adult Hepatocellular Carcinoma 24 0.030
447
c INF093 Inflammatory Bowel Disease 14 23 0.030
448
MTC055 Mitochondrial Dna Depletion Syndrome 4b 23 0.030
449
MXD019 Mixed Malaria 23 0.030
450
c ALP087 Alpha-Heavy Chain Disease 23 0.030
451
FCL001 Facial Dermatosis 23 0.030
452
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 22 0.030
453
c HYP290 Hypobetalipoproteinemia, Familial, 2 22 0.030
454
MSC012 Muscular Dystrophy, Duchenne and Becker Type 22 0.030
455
c CLC048 Celiac Disease 3 21 0.030
456
CRB087 Cerebral Arteriosclerosis 21 0.030
457
MND006 Mondor Disease 21 0.030
458
CMB002 Combat Disorder 21 0.030
459
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 21 0.030
460
SPS090 Sepsis in Premature Infants 21 0.030
461
c INF079 Inflammatory Bowel Disease 20 21 0.030
462
c CRN174 Coronary Heart Disease 2 20 0.030
463
c RNL016 Renal Infectious Disease 20 0.030
464
c CLC037 Celiac Disease 4 20 0.030
465
CNG101 Congenital Human Immunodeficiency Virus 19 0.030
466
VSC049 Visceral Myopathy, Familial, with External Ophthalmoplegia 19 0.030
467
GLT030 Gluten Allergy 19 0.030
468
c CLC039 Celiac Disease 13 18 0.030
469
PYR009 Pyridoxine Deficiency Anemia 18 0.030
470
HYP481 Hyperbiliverdinemia 17 0.030
471
c PRC033 Preeclampsia/eclampsia 3 16 0.030
472
OGL001 Ogilvie Syndrome 15 0.030
473
c KLZ002 Kala-Azar 2 14 0.030
474
CMP052 Complication in Hemodialysis 13 0.030
475
CMM018 Common Mesentery 12 0.030
476
HYP680 Hypoglossia with Situs Inversus Hypoglossia, Isolated, Included 11 0.030
477
WST006 Westphal Disease 10 0.030
478
SPL043 Split Hand, Bilateral 9 0.030