Search results for malnutrition

414 hits were found for malnutrition

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 48 7.404
2
NTR005 Nutritional Deficiency Disease 47 3.358
3
KWS001 Kwashiorkor 34 0.215
4
P DRR001 Diarrhea 59 0.197
5
MRS001 Marasmus 36 0.155
6
MLR004 Malaria 82 0.148
7
PRT036 Peritonitis 60 0.148
8
P HPT021 Hepatitis 68 0.141
9
P PNC044 Pancreatitis 60 0.125
10
P OBS005 Obesity 91 0.112
11
ATH003 Atherosclerosis 65 0.107
12
XRP001 Xerophthalmia 32 0.107
13
INS024 Insulin-Like Growth Factor I 75 0.102
14
LVR012 Liver Cirrhosis 66 0.102
15
P ANR007 Anorexia Nervosa 60 0.102
16
c DRR009 Diarrhea 6 33 0.102
17
P INF038 Influenza 71 0.097
18
P PNM007 Pneumonia 66 0.097
19
P KDN018 Kidney Disease 65 0.097
20
P THY032 Thyroiditis 53 0.097
21
c ACT004 Acute Diarrhea 37 0.097
22
P INT068 Intestinal Disease 59 0.092
23
MSL001 Measles 58 0.092
24
ASC002 Ascariasis 37 0.092
25
BNS002 Bone Structure Disease 36 0.092
26
CYS001 Cystic Fibrosis 86 0.086
27
P LVR013 Liver Disease 72 0.086
28
ISC004 Ischemia 59 0.086
29
ALC006 Alcoholic Hepatitis 58 0.086
30
ADL002 Adult Syndrome 57 0.086
31
URM002 Uremia 48 0.086
32
GRD001 Giardiasis 40 0.086
33
MSC004 Muscle Tissue Disease 37 0.086
34
P LKM002 Leukemia 72 0.079
35
TBR010 Tuberculosis 69 0.079
36
ACQ007 Acquired Immunodeficiency Syndrome 60 0.079
37
CND002 Conduct Disorder 53 0.079
38
IRN001 Iron Deficiency Anemia 51 0.079
39
P PLL002 Pellagra 40 0.079
40
TRP004 Tropical Sprue 35 0.079
41
P CLR023 Colorectal Cancer 95 0.072
42
P ART022 Arthritis 72 0.072
43
CNG034 Congestive Heart Failure 70 0.072
44
c CHR089 Chronic Kidney Failure 65 0.072
45
P GST049 Gastrointestinal System Cancer 59 0.072
46
MRB003 Morbid Obesity 58 0.072
47
P RCK004 Rickets 57 0.072
48
ETN001 Eating Disorder 56 0.072
49
CHY002 Chylomicron Retention Disease 52 0.072
50
END030 End Stage Renal Failure 51 0.072
51
VSC044 Visceral Myopathy 48 0.072
52
MTB004 Metabolic Acidosis 47 0.072
53
DYS073 Dysphagia 47 0.072
54
P NGH001 Night Blindness 47 0.072
55
CRY003 Cryptosporidiosis 46 0.072
56
P HYP729 Hypersensitivity Reaction Disease 43 0.072
57
CRB009 Cerebritis 39 0.072
58
PRT019 Protein-Losing Enteropathy 36 0.072
59
P RHM011 Rheumatoid Arthritis 87 0.065
60
P PNC035 Pancreatic Cancer 84 0.065
61
P MNN013 Meningitis 65 0.065
62
P OST002 Osteoporosis 63 0.065
63
c HPT001 Hepatitis C 62 0.065
64
c ACT073 Acute Leukemia 61 0.065
65
DFC004 Deficiency Anemia 60 0.065
66
RSP006 Respiratory System Disease 60 0.065
67
WLM001 Wolman Disease 58 0.065
68
P ORL007 Oral Cavity Cancer 57 0.065
69
KDS001 Kid Syndrome 57 0.065
70
ORL011 Oral Cancer 56 0.065
71
MCS002 Mucositis 54 0.065
72
P MSC033 Muscle Disorders 52 0.065
73
FDL002 Food Allergy 51 0.065
74
CLN019 Colonic Disease 51 0.065
75
URN009 Urinary System Disease 49 0.065
76
OVR063 Overnutrition 48 0.065
77
LCT002 Lactose Intolerance 43 0.065
78
BLD054 Blood Protein Disease 39 0.065
79
ADJ001 Adjustment Disorder 38 0.065
80
c DRR007 Diarrhea 7 30 0.065
81
P NRB001 Neuroblastoma 71 0.056
82
P CLC005 Celiac Disease 69 0.056
83
P CRD011 Cardiomyopathy 67 0.056
84
LSH001 Leishmaniasis 66 0.056
85
MTH009 Mouth Disease 62 0.056
86
P INF037 Inflammatory Bowel Disease 62 0.056
87
LNG099 Lung Disease 61 0.056
88
CHL071 Child Syndrome 59 0.056
89
P ESP024 Esophagitis 59 0.056
90
c VRL010 Viral Hepatitis 58 0.056
91
WLL006 Wells Syndrome 58 0.056
92
P HYP060 Hyperinsulinism 57 0.056
93
NTH001 Netherton Syndrome 55 0.056
94
VSC003 Visceral Leishmaniasis 55 0.056
95
CSY001 C Syndrome 53 0.056
96
P SPS003 Spastic Diplegia 52 0.056
97
BRN106 Burns 52 0.056
98
BNF002 Bone Fracture 51 0.056
99
MCR094 Microvillus Inclusion Disease 50 0.056
100
P MSC003 Muscular Atrophy 49 0.056
101
HYP037 Hyperhomocysteinemia 49 0.056
102
GDS001 Good Syndrome 46 0.056
103
SCR002 Scurvy 43 0.056
104
c HMG003 Hemoglobin E Disease 43 0.056
105
BRN080 Brain Ischemia 40 0.056
106
DYS015 Dysentery 39 0.056
107
FNC002 Functional Diarrhea 39 0.056
108
PSD029 Pseudocholinesterase Deficiency 38 0.056
109
RCT017 Rectal Disease 38 0.056
110
c CNG413 Congenital Short Bowel Syndrome 37 0.056
111
IMP003 Impaired Renal Function Disease 36 0.056
112
BRB001 Beriberi 36 0.056
113
c HMG004 Hemoglobin D Disease 33 0.056
114
BTN004 Biotin Deficiency 33 0.056
115
CHR028 Chronic Wasting Disease 32 0.056
116
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 24 0.056
117
BNM008 Bone Mineral Density, Low 17 0.056
118
P LNG032 Lung Cancer 94 0.046
119
P HPT023 Hepatocellular Carcinoma 89 0.046
120
P HRT032 Heart Disease 75 0.046
121
c DLT002 Dilated Cardiomyopathy 74 0.046
122
CRH001 Crohn's Disease 73 0.046
123
P SCH015 Schizophrenia 71 0.046
124
P NRV007 Nervous System Disease 70 0.046
125
P LYM026 Lymphoblastic Leukemia 60 0.046
126
TTN003 Tetanus 60 0.046
127
VRL011 Viral Infectious Disease 59 0.046
128
P MCR010 Microcephaly 58 0.046
129
ART021 Arteriosclerosis 57 0.046
130
P CTR002 Cataract 57 0.046
131
P NRP001 Neuropathy 57 0.046
132
SCH014 Schistosomiasis 56 0.046
133
c PRC016 Pre-Eclampsia 56 0.046
134
PNC034 Pancreas Disease 55 0.046
135
P PRC031 Preeclampsia/eclampsia 1 55 0.046
136
c PND001 Pain Disorder 55 0.046
137
GST050 Gastrointestinal System Disease 53 0.046
138
c BCT007 Bacterial Meningitis 53 0.046
139
LYS003 Lysinuric Protein Intolerance 53 0.046
140
GST037 Gastroparesis 52 0.046
141
P ENC018 Encephalopathy 52 0.046
142
MNT002 Mental Depression 52 0.046
143
GTR002 Goiter 52 0.046
144
DMN002 Dementia 52 0.046
145
END035 Endocrine Gland Cancer 50 0.046
146
PRC012 Pericardial Effusion 50 0.046
147
BRN071 Brain Injury 50 0.046
148
MSC072 Muscle Cancer 50 0.046
149
MSS002 Mass Syndrome 49 0.046
150
KRT002 Keratomalacia 49 0.046
151
CRD002 Cri-Du-Chat Syndrome 49 0.046
152
ALC009 Alcoholic Liver Cirrhosis 48 0.046
153
P SHR001 Short Bowel Syndrome 47 0.046
154
PRT030 Parathyroid Gland Disease 47 0.046
155
c FRC011 Fructose Intolerance, Hereditary 46 0.046
156
TBR011 Tuberculous Meningitis 46 0.046
157
c CLR085 Colorectal Cancer 1 46 0.046
158
DNT012 Dental Caries 46 0.046
159
GLC008 Glucose Metabolism Disease 44 0.046
160
c HMG001 Hemoglobin C Disease 44 0.046
161
RPR002 Reproductive System Disease 43 0.046
162
AMB001 Amebiasis 43 0.046
163
PHY002 Physical Disorder 43 0.046
164
WRN003 Wernicke Encephalopathy 43 0.046
165
PRS036 Parasitic Protozoa Infectious Disease 42 0.046
166
EXC002 Exocrine Pancreatic Insufficiency 42 0.046
167
SXL003 Sexual Disorder 42 0.046
168
END038 Endocrine Pancreas Disease 42 0.046
169
FTL021 Fetal Macrosomia 41 0.046
170
ANC001 Ancylostomiasis 41 0.046
171
TRC023 Trichinosis 41 0.046
172
DNT001 Dental Fluorosis 40 0.046
173
GST009 Gastroschisis 40 0.046
174
P CRB088 Cerebral Atrophy 39 0.046
175
NCR001 Necrotizing Ulcerative Gingivitis 38 0.046
176
c HYP058 Hypervitaminosis a 37 0.046
177
MTC061 Mitochondrial Dna Depletion Syndrome 1 36 0.046
178
c PNC111 Pancreatic Cancer 2 29 0.046
179
c PNC094 Pancreatic Cancer 1 27 0.046
180
MTC055 Mitochondrial Dna Depletion Syndrome 4b 25 0.046
181
VSC049 Visceral Myopathy, Familial, with External Ophthalmoplegia 22 0.046
182
ADS015 Aids Wasting Syndrome 19 0.046
183
NDD001 Nodding Syndrome 17 0.046
184
HYP727 Hypoglossia with Situs Inversus 14 0.046
185
c SYS001 Systemic Lupus Erythematosus 86 0.032
186
HV1006 Hiv-1 80 0.032
187
P DBT085 Diabetes Mellitus, Insulin-Dependent 79 0.032
188
DCH001 Duchenne Muscular Dystrophy 79 0.032
189
P CRN211 Coronary Artery Disease 73 0.032
190
P HMC003 Hemochromatosis 72 0.032
191
SCK003 Sickle Cell Anemia 71 0.032
192
BCK001 Becker Muscular Dystrophy 71 0.032
193
c HPT073 Hepatitis C Virus 70 0.032
194
SQM006 Squamous Cell Carcinoma 69 0.032
195
P LYM118 Lymphoma 69 0.032
196
PCK002 Pick Disease 68 0.032
197
P ANR002 Aniridia 66 0.032
198
CHG001 Chagas Disease 66 0.032
199
P NSP012 Nasopharyngeal Carcinoma 66 0.032
200
CHD001 Chediak-Higashi Syndrome 65 0.032
201
VSC007 Vascular Disease 65 0.032
202
P CRD013 Cardiofaciocutaneous Syndrome 65 0.032
203
P TRN020 Turner Syndrome 65 0.032
204
P MSC005 Muscular Dystrophy 65 0.032
205
SKN016 Skin Disease 64 0.032
206
OBS002 Obsessive-Compulsive Disorder 64 0.032
207
P AMY004 Amyloidosis 64 0.032
208
P LPS004 Lupus Erythematosus 63 0.032
209
PLM001 Pulmonary Tuberculosis 63 0.032
210
CRB039 Cerebrovascular Disease 63 0.032
211
c HPT016 Hepatitis B 62 0.032
212
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.032
213
P THL005 Thalassemia 61 0.032
214
RBR001 Roberts Syndrome 61 0.032
215
BLM001 Bloom Syndrome 61 0.032
216
P ENC004 Encephalitis 61 0.032
217
OVR029 Ovarian Hyperstimulation Syndrome 61 0.032
218
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.032
219
GNG013 Gingivitis 61 0.032
220
HYP056 Hypoglycemia 60 0.032
221
c CNT035 Central Nervous System Disease 60 0.032
222
HYP066 Hyperglycemia 59 0.032
223
P NRV006 Nervous System Cancer 59 0.032
224
APP008 Appendicitis 59 0.032
225
P HRS035 Hirschsprung Disease 1 58 0.032
226
STT001 Status Epilepticus 58 0.032
227
CTS003 Coats Disease 58 0.032
228
ZLL001 Zellweger Syndrome 58 0.032
229
GST045 Gastroenteritis 57 0.032
230
IRR002 Irritable Bowel Syndrome 57 0.032
231
P ALC004 Alcohol Abuse 57 0.032
232
c PNC108 Pancreatitis, Hereditary 57 0.032
233
P EXN002 Exanthem 57 0.032
234
LPD008 Lipid Metabolism Disorder 57 0.032
235
P HYP069 Hyperparathyroidism 56 0.032
236
c HPT003 Hepatitis a 56 0.032
237
P CND004 Candidiasis 56 0.032
238
c HRD002 Hereditary Angioedema 56 0.032
239
ART111 Artery Disease 55 0.032
240
HYP266 Hypoxia 55 0.032
241
BLD034 Bile Duct Carcinoma 55 0.032
242
WLM007 Wilms Tumor Susceptibility-5 55 0.032
243
GLC003 Glucose Intolerance 54 0.032
244
P DGR001 Digeorge Syndrome 54 0.032
245
PLS007 Plasmodium Falciparum Malaria 54 0.032
246
c MSC124 Muscular Dystrophy, Congenital 54 0.032
247
P HYP083 Hypopituitarism 54 0.032
248
P HYP076 Hyperthyroidism 53 0.032
249
P LPD010 Lipodystrophy 53 0.032
250
P FTL001 Fetal Alcohol Syndrome 53 0.032
251
PLC005 Placental Insufficiency 53 0.032
252
IMM136 Immune System Disease 53 0.032
253
ISC006 Ischemic Heart Disease 53 0.032
254
DSS008 Disease of Mental Health 53 0.032
255
THL018 Thalassemia Major 52 0.032
256
P ANG015 Angioedema 52 0.032
257
EXT034 Extrinsic Allergic Alveolitis 52 0.032
258
P PLY014 Polycystic Kidney Disease 52 0.032
259
PLS006 Plasmodium Vivax Malaria 52 0.032
260
SHG001 Shigellosis 52 0.032
261
CYS005 Cysticercosis 52 0.032
262
CHL014 Cholera 52 0.032
263
c VRL007 Viral Encephalitis 51 0.032
264
P ECL001 Eclampsia 51 0.032
265
BCT002 Bacterial Vaginosis 51 0.032
266
P TRC086 Trichohepatoenteric Syndrome 1 51 0.032
267
URC002 Urea Cycle Disorder 51 0.032
268
P GND004 Gonadal Dysgenesis 51 0.032
269
MYC002 Mycobacterium Avium Complex Disease 51 0.032
270
SLM003 Salmonellosis 51 0.032
271
OCL008 Oculopharyngeal Muscular Dystrophy 50 0.032
272
VND002 Van Der Woude Syndrome 50 0.032
273
P PRC019 Precocious Puberty 50 0.032
274
PRL032 Perlman Syndrome 50 0.032
275
PNC001 Pancytopenia 49 0.032
276
PMP001 Pemphigus 49 0.032
277
PRT011 Protein C Deficiency 49 0.032
278
VND001 Vein Disease 49 0.032
279
RTN023 Retinitis 49 0.032
280
ONC002 Onchocerciasis 48 0.032
281
HYP077 Hypertrichosis 48 0.032
282
SCH012 Schizoaffective Disorder 48 0.032
283
PRP021 Peripheral Nervous System Neoplasm 48 0.032
284
OBS001 Obstructive Jaundice 48 0.032
285
STM006 Stomach Disease 47 0.032
286
c HPT015 Hepatitis D 47 0.032
287
ACH005 Achalasia 47 0.032
288
SKN023 Skin Tag 46 0.032
289
P TCL004 T-Cell Leukemia 46 0.032
290
P PRD008 Periodontitis 46 0.032
291
SCB001 Scabies 46 0.032
292
LKC003 Leukocyte Disease 46 0.032
293
MGC001 Megacolon 46 0.032
294
c AMY009 Amyloidosis Aa 45 0.032
295
TRC008 Trachoma 45 0.032
296
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.032
297
CRD118 Cardiovascular Cancer 45 0.032
298
DWR001 Dwarfism 45 0.032
299
HMS001 Hemosiderosis 44 0.032
300
c ADL096 Adult Hepatocellular Carcinoma 44 0.032
301
P SDR002 Siderosis 44 0.032
302
BCT004 Bacteriuria 44 0.032
303
HPT074 Hepatic Adenoma, Somatic 44 0.032
304
NSY001 N Syndrome 44 0.032
305
BRT030 Birth Defects 44 0.032
306
SKN027 Skin Conditions 44 0.032
307
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 43 0.032
308
CRR007 Cirrhosis, Cryptogenic 43 0.032
309
GLS007 Glossitis 43 0.032
310
MLK006 Milk Allergy 43 0.032
311
IRN002 Iron Metabolism Disease 42 0.032
312
HYP085 Hypothalamic Disease 42 0.032
313
IMP004 Impetigo 42 0.032
314
ANM001 Anemia of Prematurity 42 0.032
315
MCR017 Macrocytic Anemia 42 0.032
316
HYP081 Hypolipoproteinemia 42 0.032
317
NM001 Noma 42 0.032
318
END072 Endotheliitis 41 0.032
319
ATN003 Autonomic Nervous System Neoplasm 41 0.032
320
VGN020 Vaginal Disease 41 0.032
321
c INT072 Intestinal Pseudo-Obstruction 41 0.032
322
P HVY001 Heavy Chain Disease 40 0.032
323
P ACQ009 Acquired Metabolic Disease 40 0.032
324
AMN006 Aminoaciduria 40 0.032
325
c PRG106 Progressive Muscular Dystrophy 40 0.032
326
SPR007 Superior Mesenteric Artery Syndrome 40 0.032
327
MNR003 Mineral Metabolism Disease 40 0.032
328
STT004 Steatorrhea 40 0.032
329
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 39 0.032
330
PYM001 Pyomyositis 38 0.032
331
MCR020 Microsporidiosis 38 0.032
332
ALC010 Alcoholic Cardiomyopathy 38 0.032
333
ASP004 Asphyxia Neonatorum 38 0.032
334
CNT025 Central Pontine Myelinolysis 38 0.032
335
SPC003 Specific Developmental Disorder 38 0.032
336
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 38 0.032
337
TRC077 Trichomegaly 38 0.032
338
GNR003 Generalized Atherosclerosis 37 0.032
339
P FML187 Familial Hypertension 37 0.032
340
TNS007 Taeniasis 37 0.032
341
P RTN022 Retinal Vein Occlusion 37 0.032
342
SNL007 Senile Cataract 37 0.032
343
ANR018 Anorchia 37 0.032
344
C1N001 C1 Inhibitor Deficiency 36 0.032
345
MRG013 Mirage Syndrome 36 0.032
346
c HYP311 Hyperparathyroidism 3 36 0.032
347
PYR016 Pyridoxine Deficiency 35 0.032
348
ACR005 Acrodermatitis 35 0.032
349
c CNT016 Central Retinal Vein Occlusion 35 0.032
350
c CRD187 Cardiomyopathy, Dilated, 3b 35 0.032
351
FLC001 Folic Acid Deficiency Anemia 35 0.032
352
ACD004 Acdc 35 0.032
353
NNT011 Neonatal Anemia 35 0.032
354
ECT004 Ecthyma 34 0.032
355
IMM068 Immunodeficiency 8 34 0.032
356
DDN007 Duodenal Disease 34 0.032
357
SKL007 Skeletal Muscle Regeneration 33 0.032
358
RFR013 Refractory Celiac Disease 33 0.032
359
PST010 Pasteurellosis 32 0.032
360
WHT017 Wheat Allergy 32 0.032
361
PYR004 Pyuria 31 0.032
362
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 31 0.032
363
TMP011 Temple-Baraitser Syndrome 31 0.032
364
ANS012 Anus Disease 31 0.032
365
CHY005 Chylothorax, Congenital 31 0.032
366
BRL001 Brill-Zinsser Disease 31 0.032
367
VTM003 Vitamin Metabolic Disorder 31 0.032
368
MCL072 Macular Dystrophy, North Carolina Type 30 0.032
369
c HMG029 Hemoglobin Se Disease 30 0.032
370
c INF002 Inflammatory Diarrhea 30 0.032
371
ALR002 Al-Raqad Syndrome 29 0.032
372
FSH003 Fish Allergy 29 0.032
373
NSP003 Nasopharyngeal Disease 28 0.032
374
ISC016 Ischiocoxopodopatellar Syndrome 28 0.032
375
P KLZ004 Kala-Azar 1 28 0.032
376
SCR037 Sucrase-Isomaltase Deficiency, Congenital 28 0.032
377
P PLT008 Pili Torti 27 0.032
378
ATR073 Atrophic Glossitis 27 0.032
379
OST097 Osteoporotic Fracture 27 0.032
380
c ANR038 Anorexia Nervosa 1 27 0.032
381
PMP008 Pemphigus Vegetans 26 0.032
382
5XP001 5-Oxoprolinase Deficiency 26 0.032
383
NLL002 Null Syndrome 26 0.032
384
OSM001 Osmotic Diarrhea 26 0.032
385
MSC012 Muscular Dystrophy, Duchenne and Becker Type 25 0.032
386
c ALP087 Alpha-Heavy Chain Disease 25 0.032
387
c CLC048 Celiac Disease 3 24 0.032
388
FCL001 Facial Dermatosis 24 0.032
389
CMB002 Combat Disorder 24 0.032
390
c NSP009 Nasopharyngeal Carcinoma 2 23 0.032
391
c NSP015 Nasopharyngeal Carcinoma 3 23 0.032
392
c INF093 Inflammatory Bowel Disease 14 23 0.032
393
c HYP290 Hypobetalipoproteinemia, Familial, 2 23 0.032
394
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 22 0.032
395
MXD019 Mixed Malaria 22 0.032
396
c CRN214 Coronary Heart Disease 5 22 0.032
397
MND006 Mondor Disease 22 0.032
398
c INF079 Inflammatory Bowel Disease 20 22 0.032
399
P INT103 Intrauterine Infections 21 0.032
400
c CLC037 Celiac Disease 4 21 0.032
401
c CRN174 Coronary Heart Disease 2 21 0.032
402
SPS090 Sepsis in Premature Infants 21 0.032
403
CNG101 Congenital Human Immunodeficiency Virus 20 0.032
404
c CLC039 Celiac Disease 13 19 0.032
405
GLT030 Gluten Allergy 19 0.032
406
HYP481 Hyperbiliverdinemia 19 0.032
407
TRN068 Transketolase Deficiency 16 0.032
408
OGL001 Ogilvie Syndrome 15 0.032
409
CMP052 Complication in Hemodialysis 15 0.032
410
c KLZ002 Kala-Azar 2 15 0.032
411
CMM018 Common Mesentery 14 0.032
412
c MTR062 Maternal Uniparental Disomy of Chromosome 4 14 0.032
413
SPL043 Split Hand, Bilateral 10 0.032
414
WST006 Westphal Disease 10 0.032
Content
Loading form....