Search results for "malnutrition"

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

293 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 47 7.572
2
PRC002 Paracoccidioidomycosis 67 2.701
3
KWS001 Kwashiorkor 47 0.223
4
PRT036 Peritonitis 71 0.170
5
c HPT021 Hepatitis 63 0.153
6
MRS001 Marasmus 46 0.144
7
c PNC044 Pancreatitis 68 0.129
8
XRP001 Xerophthalmia 37 0.123
9
P OBS005 Obesity 89 0.118
10
c DRR001 Diarrhea 51 0.118
11
P MLR004 Malaria 74 0.111
12
P ANR007 Anorexia Nervosa 65 0.111
13
c THY032 Thyroiditis 65 0.111
14
LVR012 Liver Cirrhosis 76 0.105
15
c DBT009 Diabetes Mellitus 73 0.105
16
ATH003 Atherosclerosis 68 0.105
17
ASC002 Ascariasis 46 0.105
18
CYS001 Cystic Fibrosis 96 0.098
19
ALC006 Alcoholic Hepatitis 57 0.098
20
URM002 Uremia 57 0.098
21
GRD001 Giardiasis 56 0.098
22
P PLL002 Pellagra 54 0.098
23
P LKM002 Leukemia 76 0.091
24
ISC004 Ischemia 62 0.091
25
TRP004 Tropical Sprue 37 0.091
26
P ART022 Arthritis 74 0.083
27
MSL001 Measles 67 0.083
28
P INS005 Insulin Resistance 64 0.083
29
PRT019 Protein-Losing Enteropathy 55 0.083
30
MTB004 Metabolic Acidosis 45 0.083
31
CRB009 Cerebritis 38 0.083
32
P RHM011 Rheumatoid Arthritis 94 0.074
33
TBR010 Tuberculosis 85 0.074
34
P RCK004 Rickets 67 0.074
35
c KDN018 Kidney Disease 62 0.074
36
c ACT073 Acute Leukemia 56 0.074
37
DYS073 Dysphagia 51 0.074
38
P LCT002 Lactose Intolerance 48 0.074
39
ANC001 Ancylostomiasis 39 0.074
40
CRH001 Crohn's Disease 75 0.064
41
ACQ007 Acquired Immunodeficiency Syndrome 70 0.064
42
P NRB001 Neuroblastoma 70 0.064
43
P LVR013 Liver Disease 68 0.064
44
c MNN013 Meningitis 67 0.064
45
MRB003 Morbid Obesity 67 0.064
46
P ESP024 Esophagitis 63 0.064
47
CRB021 Cerebral Malaria 59 0.064
48
ETN001 Eating Disorder 56 0.064
49
FDL002 Food Allergy 52 0.064
50
HYP037 Hyperhomocysteinemia 52 0.064
51
BRN080 Brain Ischemia 50 0.064
52
DYS015 Dysentery 50 0.064
53
OVR063 Overnutrition 48 0.064
54
c NGH001 Night Blindness 48 0.064
55
DBT061 Diabetic Nephropathy 47 0.064
56
BRB001 Beriberi 45 0.064
57
c ACT004 Acute Diarrhea 44 0.064
58
BTN004 Biotin Deficiency 41 0.064
59
P DLT002 Dilated Cardiomyopathy 87 0.053
60
P HYP075 Hypertension 85 0.053
61
P SCH015 Schizophrenia 84 0.053
62
P LNG032 Lung Cancer 78 0.053
63
CNG034 Congestive Heart Failure 77 0.053
64
P PNM007 Pneumonia 77 0.053
65
LSH001 Leishmaniasis 73 0.053
66
SCH014 Schistosomiasis 72 0.053
67
P INF038 Influenza 67 0.053
68
c JVN010 Juvenile Rheumatoid Arthritis 67 0.053
69
GST009 Gastroschisis 66 0.053
70
P WLM002 Wilms Tumor 66 0.053
71
P CHR089 Chronic Kidney Failure 65 0.053
72
TTN003 Tetanus 64 0.053
73
P ACT101 Acute Lymphoblastic Leukemia 64 0.053
74
c VRL010 Viral Hepatitis 63 0.053
75
DFC004 Deficiency Anemia 62 0.053
76
P GTR002 Goiter 61 0.053
77
NRP001 Neuropathy 61 0.053
78
VSC003 Visceral Leishmaniasis 60 0.053
79
AMB001 Amebiasis 59 0.053
80
TBR011 Tuberculous Meningitis 58 0.053
81
PRC012 Pericardial Effusion 57 0.053
82
END030 End Stage Renal Failure 57 0.053
83
PRT039 Proteinuria 57 0.053
84
P SDR002 Siderosis 57 0.053
85
BRN071 Brain Injury 57 0.053
86
c CTR002 Cataract 57 0.053
87
IRN001 Iron Deficiency Anemia 56 0.053
88
c LYM026 Lymphoblastic Leukemia 56 0.053
89
c HYP060 Hyperinsulinism 56 0.053
90
P CHR409 Chronic Obstructive Pulmonary Disease 54 0.053
91
P INT072 Intestinal Pseudo-Obstruction 53 0.053
92
BLN003 Blindness 52 0.053
93
ALC009 Alcoholic Liver Cirrhosis 51 0.053
94
OBS001 Obstructive Jaundice 50 0.053
95
BRN106 Burns 49 0.053
96
MCR094 Microvillus Inclusion Disease 49 0.053
97
DNT001 Dental Fluorosis 48 0.053
98
DNT012 Dental Caries 48 0.053
99
P HYP058 Hypervitaminosis a 48 0.053
100
KRT002 Keratomalacia 47 0.053
101
P CRB088 Cerebral Atrophy 46 0.053
102
FTL021 Fetal Macrosomia 44 0.053
103
c INF037 Inflammatory Bowel Disease 43 0.053
104
HLM001 Helminthiasis 42 0.053
105
TRC023 Trichinosis 39 0.053
106
VSC044 Visceral Myopathy 37 0.053
107
NTR005 Nutritional Deficiency Disease 33 0.053
108
NCR001 Necrotizing Ulcerative Gingivitis 30 0.053
109
P ALZ001 Alzheimer's Disease 98 0.037
110
P LVR011 Liver Cancer 90 0.037
111
P SYS001 Systemic Lupus Erythematosus 89 0.037
112
P ATX002 Ataxia Telangiectasia 87 0.037
113
P HMC003 Hemochromatosis 85 0.037
114
GLC006 Galactosemia 85 0.037
115
SCK003 Sickle Cell Anemia 84 0.037
116
AND002 Androgen Insensitivity Syndrome 80 0.037
117
P PRC016 Pre-Eclampsia 79 0.037
118
c NNN003 Noonan Syndrome 79 0.037
119
P CLR023 Colorectal Cancer 77 0.037
120
BRK003 Burkitt's Lymphoma 77 0.037
121
LRN002 Laron Syndrome 77 0.037
122
P OST002 Osteoporosis 76 0.037
123
CHD001 Chediak-Higashi Syndrome 76 0.037
124
ANK002 Ankylosing Spondylitis 76 0.037
125
c LPS004 Lupus Erythematosus 75 0.037
126
P CLC005 Celiac Disease 74 0.037
127
BLM001 Bloom Syndrome 74 0.037
128
P WGN002 Wegener's Granulomatosis 73 0.037
129
P AMY004 Amyloidosis 73 0.037
130
ADN001 Adenosine Deaminase Deficiency 73 0.037
131
c PRM002 Primary Hyperoxaluria 73 0.037
132
P HYP458 Hyper Ige Syndrome 72 0.037
133
OBS002 Obsessive-Compulsive Disorder 71 0.037
134
P ANG001 Angelman Syndrome 71 0.037
135
c THL005 Thalassemia 71 0.037
136
DBT011 Diabetic Retinopathy 70 0.037
137
c AXN002 Axenfeld-Rieger Syndrome 69 0.037
138
P MTB001 Metabolic Syndrome X 69 0.037
139
VSC007 Vascular Disease 69 0.037
140
c ACT074 Acute Lymphocytic Leukemia 69 0.037
141
TRC008 Trachoma 69 0.037
142
SPS077 Sepsis 69 0.037
143
P CNG401 Congenital Heart Disease 69 0.037
144
c HPT016 Hepatitis B 68 0.037
145
P PRD008 Periodontitis 68 0.037
146
P HRD011 Hereditary Spherocytosis 68 0.037
147
LYS003 Lysinuric Protein Intolerance 68 0.037
148
P PLY011 Polycystic Ovary Syndrome 67 0.037
149
OVR029 Ovarian Hyperstimulation Syndrome 67 0.037
150
ART021 Arteriosclerosis 67 0.037
151
P DGR001 Digeorge Syndrome 67 0.037
152
P MCL015 Mucolipidosis Ii 67 0.037
153
c NPH012 Nephrotic Syndrome 67 0.037
154
P CRD013 Cardiofaciocutaneous Syndrome 66 0.037
155
STF001 Stiff-Person Syndrome 66 0.037
156
P HYP056 Hypoglycemia 66 0.037
157
P HPT001 Hepatitis C 66 0.037
158
TRN001 Transthyretin Amyloidosis 65 0.037
159
STT001 Status Epilepticus 65 0.037
160
P OVR049 Ovarian Disease 64 0.037
161
SHG001 Shigellosis 64 0.037
162
OCL008 Oculopharyngeal Muscular Dystrophy 64 0.037
163
ACN002 Acanthosis Nigricans 64 0.037
164
CHL014 Cholera 64 0.037
165
c ECL001 Eclampsia 63 0.037
166
BTN003 Biotinidase Deficiency 63 0.037
167
ART019 Aortic Valve Stenosis 63 0.037
168
CRY003 Cryptosporidiosis 63 0.037
169
c GLL020 Gallbladder Disease 63 0.037
170
HV1006 Hiv-1 63 0.037
171
c HYP076 Hyperthyroidism 62 0.037
172
CMP002 Campylobacteriosis 62 0.037
173
RBS003 Rabson-Mendenhall Syndrome 62 0.037
174
CHG001 Chagas Disease 62 0.037
175
CYS005 Cysticercosis 62 0.037
176
TYP007 Typhoid Fever 62 0.037
177
c CND004 Candidiasis 61 0.037
178
HYP066 Hyperglycemia 61 0.037
179
MYL020 Myelomeningocele 61 0.037
180
c FML012 Familial Partial Lipodystrophy 61 0.037
181
GLC003 Glucose Intolerance 61 0.037
182
GNG013 Gingivitis 60 0.037
183
PLM001 Pulmonary Tuberculosis 60 0.037
184
SCB001 Scabies 60 0.037
185
SCR002 Scurvy 59 0.037
186
MGC001 Megacolon 59 0.037
187
BLM002 Bulimia Nervosa 58 0.037
188
LPD010 Lipodystrophy 58 0.037
189
BCT004 Bacteriuria 58 0.037
190
P INT068 Intestinal Disease 57 0.037
191
c CNT016 Central Retinal Vein Occlusion 57 0.037
192
HYP266 Hypoxia 57 0.037
193
HMS001 Hemosiderosis 57 0.037
194
INS008 Insulin-Like Growth Factor I Deficiency 56 0.037
195
P RTN022 Retinal Vein Occlusion 56 0.037
196
c MCR010 Microcephaly 56 0.037
197
ART001 Arterial Tortuosity Syndrome 55 0.037
198
VND002 Van Der Woude Syndrome 55 0.037
199
CRD005 Cardia Cancer 55 0.037
200
ACR005 Acrodermatitis 55 0.037
201
PRM003 Premature Ejaculation 54 0.037
202
HPT023 Hepatocellular Carcinoma 54 0.037
203
c ACR001 Aicardi-Goutieres Syndrome 54 0.037
204
SCH012 Schizoaffective Disorder 53 0.037
205
STT004 Steatorrhea 53 0.037
206
HYP077 Hypertrichosis 53 0.037
207
RTN023 Retinitis 53 0.037
208
YLL001 Yellow Nail Syndrome 53 0.037
209
AND003 Andersen-Tawil Syndrome 53 0.037
210
P MSC003 Muscular Atrophy 53 0.037
211
GST045 Gastroenteritis 53 0.037
212
THR013 Thoracic Outlet Syndrome 52 0.037
213
P HYP083 Hypopituitarism 52 0.037
214
CHY002 Chylomicron Retention Disease 52 0.037
215
c CNG012 Congenital Generalized Lipodystrophy 52 0.037
216
NM001 Noma 52 0.037
217
P PRP023 Peripheral Neuropathy 51 0.037
218
ESN005 Eosinophilic Gastroenteritis 51 0.037
219
ONC002 Onchocerciasis 51 0.037
220
URC002 Urea Cycle Disorder 51 0.037
221
GLS007 Glossitis 51 0.037
222
HVD003 Hiv/aids 51 0.037
223
AMY053 Amyloidosis, Secondary 51 0.037
224
SHR001 Short Bowel Syndrome 51 0.037
225
P ALC004 Alcohol Abuse 51 0.037
226
LPD004 Lipoid Nephrosis 50 0.037
227
P CST002 Castleman's Disease 50 0.037
228
END072 Endotheliitis 50 0.037
229
ATX019 Ataxia with Vitamin E Deficiency 50 0.037
230
c TCL004 T-Cell Leukemia 50 0.037
231
SMT019 Somatostatin Analog 50 0.037
232
MCR020 Microsporidiosis 49 0.037
233
P NRV007 Nervous System Disease 49 0.037
234
c BCT007 Bacterial Meningitis 49 0.037
235
c SVR005 Severe Pre-Eclampsia 49 0.037
236
IMP004 Impetigo 49 0.037
237
ALC010 Alcoholic Cardiomyopathy 49 0.037
238
EXC002 Exocrine Pancreatic Insufficiency 48 0.037
239
TRN022 Transcobalamin Ii Deficiency 48 0.037
240
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 47 0.037
241
P ATX010 Ataxia Neuropathy Spectrum 47 0.037
242
FBR063 Fibrocalculous Pancreatic Diabetes 46 0.037
243
CNT025 Central Pontine Myelinolysis 46 0.037
244
BNF002 Bone Fracture 45 0.037
245
MCR017 Macrocytic Anemia 45 0.037
246
c FTL001 Fetal Alcohol Syndrome 44 0.037
247
LPT005 Leptin Deficiency 44 0.037
248
FTT001 Fatty Liver Disease 44 0.037
249
PLC005 Placental Insufficiency 43 0.037
250
AMN006 Aminoaciduria 43 0.037
251
HYP029 Hyperthyroxinemia 43 0.037
252
SNL007 Senile Cataract 42 0.037
253
P HRD013 Hereditary Fructose Intolerance Syndrome 41 0.037
254
5FL001 5-Fluorouracil Toxicity 41 0.037
255
WRN003 Wernicke Encephalopathy 40 0.037
256
ESP028 Esophageal Squamous Cell Carcinoma 40 0.037
257
P EPD044 Epidermolysis Bullosa Dystrophica, Ar 40 0.037
258
c HVY001 Heavy Chain Disease 39 0.037
259
SML020 Small Patella Syndrome 38 0.037
260
PLT008 Pili Torti 38 0.037
261
VRL011 Viral Infectious Disease 38 0.037
262
c MLR021 Malaria, Severe 38 0.037
263
SPR066 Superficial Siderosis 38 0.037
264
NRT005 North Carolina Macular Dystrophy 37 0.037
265
c HYP290 Hypobetalipoproteinemia, Familial, 2 36 0.037
266
IPX001 Ipex Syndrome 36 0.037
267
DYS070 Dysalbuminemic Hyperthyroxinemia 35 0.037
268
PYR016 Pyridoxine Deficiency 35 0.037
269
PSD029 Pseudocholinesterase Deficiency 34 0.037
270
SYN053 Syndromic Diarrhea 34 0.037
271
CNG127 Congenital Sucrase-Isomaltase Deficiency 33 0.037
272
c ATS059 Autosomal Dominant Hyper Ige Syndrome 31 0.037
273
c ALP060 Alpha Heavy-Chain Disease 30 0.037
274
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.037
275
ANK010 Ankylostomiasis 29 0.037
276
HNM002 Hinman Syndrome 28 0.037
277
PYR004 Pyuria 28 0.037
278
TFT003 Tufting Enteropathy 28 0.037
279
TNS007 Taeniasis 28 0.037
280
ECT004 Ecthyma 27 0.037
281
IRN002 Iron Metabolism Disease 27 0.037
282
BNT002 Bantu Siderosis 26 0.037
283
ATR073 Atrophic Glossitis 23 0.037
284
MNT002 Mental Depression 23 0.037
285
MTC061 Mitochondrial Dna Depletion Syndrome 1 22 0.037
286
c BNG076 Benign Exophthalmos Syndrome 22 0.037
287
FML093 Familial Visceral Myopathy with External Ophthalmoplegia 21 0.037
288
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 20 0.037
289
HYP081 Hypolipoproteinemia 19 0.037
290
BRL001 Brill-Zinsser Disease 19 0.037
291
HYP481 Hyperbiliverdinemia 17 0.037
292
MTC055 Mitochondrial Dna Depletion Syndrome 4b 13 0.037
293
ISL031 Isolated Congenital Hypoglossia/aglossia 12 0.037