Search results for "malnutrition"

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

279 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 45 7.572
2
PRC002 Paracoccidioidomycosis 64 2.700
3
KWS001 Kwashiorkor 46 0.227
4
PRT036 Peritonitis 71 0.173
5
c HPT021 Hepatitis 64 0.156
6
MRS001 Marasmus 44 0.151
7
c PNC044 Pancreatitis 69 0.125
8
XRP001 Xerophthalmia 37 0.125
9
c DRR001 Diarrhea 51 0.119
10
P OBS005 Obesity 89 0.113
11
P MLR004 Malaria 75 0.113
12
P ANR007 Anorexia Nervosa 66 0.113
13
c THY032 Thyroiditis 66 0.113
14
c DBT009 Diabetes Mellitus 78 0.107
15
LVR012 Liver Cirrhosis 75 0.107
16
ATH003 Atherosclerosis 68 0.107
17
ASC002 Ascariasis 46 0.107
18
ALC006 Alcoholic Hepatitis 57 0.100
19
GRD001 Giardiasis 55 0.100
20
P PLL002 Pellagra 53 0.100
21
CYS001 Cystic Fibrosis 96 0.093
22
P LKM002 Leukemia 77 0.093
23
URM002 Uremia 56 0.093
24
TRP004 Tropical Sprue 35 0.093
25
P ART022 Arthritis 75 0.084
26
MSL001 Measles 67 0.084
27
P INS005 Insulin Resistance 66 0.084
28
ISC004 Ischemia 63 0.084
29
PRT019 Protein-Losing Enteropathy 50 0.084
30
MTB004 Metabolic Acidosis 43 0.084
31
CRB009 Cerebritis 39 0.084
32
P RHM011 Rheumatoid Arthritis 93 0.076
33
TBR010 Tuberculosis 83 0.076
34
P RCK004 Rickets 64 0.076
35
c KDN018 Kidney Disease 62 0.076
36
c ACT073 Acute Leukemia 56 0.076
37
DYS073 Dysphagia 51 0.076
38
P LCT002 Lactose Intolerance 49 0.076
39
c NGH001 Night Blindness 48 0.076
40
ANC001 Ancylostomiasis 39 0.076
41
CRH001 Crohn's Disease 74 0.065
42
P NRB001 Neuroblastoma 70 0.065
43
P LVR013 Liver Disease 69 0.065
44
c MNN013 Meningitis 68 0.065
45
MRB003 Morbid Obesity 66 0.065
46
P ESP024 Esophagitis 63 0.065
47
ACQ007 Acquired Immunodeficiency Syndrome 61 0.065
48
CRB021 Cerebral Malaria 59 0.065
49
ETN001 Eating Disorder 57 0.065
50
BLN003 Blindness 52 0.065
51
FDL002 Food Allergy 52 0.065
52
HYP037 Hyperhomocysteinemia 51 0.065
53
DYS015 Dysentery 49 0.065
54
OVR063 Overnutrition 48 0.065
55
c ACT004 Acute Diarrhea 43 0.065
56
BRB001 Beriberi 42 0.065
57
DBT061 Diabetic Nephropathy 40 0.065
58
BTN004 Biotin Deficiency 39 0.065
59
P HYP075 Hypertension 85 0.053
60
P SCH015 Schizophrenia 82 0.053
61
P DLT002 Dilated Cardiomyopathy 82 0.053
62
HPT023 Hepatocellular Carcinoma 79 0.053
63
CNG034 Congestive Heart Failure 78 0.053
64
P PNM007 Pneumonia 76 0.053
65
LSH001 Leishmaniasis 74 0.053
66
P LNG032 Lung Cancer 72 0.053
67
SCH014 Schistosomiasis 70 0.053
68
P INF038 Influenza 68 0.053
69
c JVN010 Juvenile Rheumatoid Arthritis 65 0.053
70
P CHR089 Chronic Kidney Failure 65 0.053
71
c VRL010 Viral Hepatitis 64 0.053
72
TTN003 Tetanus 63 0.053
73
DFC004 Deficiency Anemia 62 0.053
74
P GTR002 Goiter 62 0.053
75
NRP001 Neuropathy 61 0.053
76
VSC003 Visceral Leishmaniasis 59 0.053
77
AMB001 Amebiasis 58 0.053
78
TBR011 Tuberculous Meningitis 58 0.053
79
PRC012 Pericardial Effusion 58 0.053
80
END030 End Stage Renal Failure 58 0.053
81
PRT039 Proteinuria 57 0.053
82
BRN071 Brain Injury 57 0.053
83
IRN001 Iron Deficiency Anemia 57 0.053
84
c CTR002 Cataract 57 0.053
85
c HYP060 Hyperinsulinism 55 0.053
86
c LYM026 Lymphoblastic Leukemia 54 0.053
87
P INT072 Intestinal Pseudo-Obstruction 53 0.053
88
c WLM002 Wilms Tumor 51 0.053
89
ALC009 Alcoholic Liver Cirrhosis 51 0.053
90
BRN080 Brain Ischemia 50 0.053
91
OBS001 Obstructive Jaundice 50 0.053
92
BRN106 Burns 49 0.053
93
DNT001 Dental Fluorosis 49 0.053
94
DNT012 Dental Caries 48 0.053
95
P HYP058 Hypervitaminosis a 46 0.053
96
KRT002 Keratomalacia 46 0.053
97
P INF037 Inflammatory Bowel Disease 45 0.053
98
FTL021 Fetal Macrosomia 44 0.053
99
CRB088 Cerebral Atrophy 44 0.053
100
HLM001 Helminthiasis 42 0.053
101
TRC023 Trichinosis 38 0.053
102
NCR001 Necrotizing Ulcerative Gingivitis 30 0.053
103
NTR005 Nutritional Deficiency Disease 25 0.053
104
P ALZ001 Alzheimer's Disease 97 0.038
105
P ATX002 Ataxia Telangiectasia 86 0.038
106
P SYS001 Systemic Lupus Erythematosus 85 0.038
107
GLC006 Galactosemia 81 0.038
108
AND002 Androgen Insensitivity Syndrome 80 0.038
109
P HMC003 Hemochromatosis 78 0.038
110
BRK003 Burkitt's Lymphoma 77 0.038
111
LRN002 Laron Syndrome 76 0.038
112
P ACT074 Acute Lymphocytic Leukemia 75 0.038
113
P OST002 Osteoporosis 75 0.038
114
P CLC005 Celiac Disease 74 0.038
115
ANK002 Ankylosing Spondylitis 74 0.038
116
PRC016 Pre-Eclampsia 74 0.038
117
BLM001 Bloom Syndrome 74 0.038
118
c NNN003 Noonan Syndrome 73 0.038
119
P CLR023 Colorectal Cancer 73 0.038
120
c LPS004 Lupus Erythematosus 72 0.038
121
c PRM002 Primary Hyperoxaluria 72 0.038
122
SCK003 Sickle Cell Anemia 72 0.038
123
c THL005 Thalassemia 72 0.038
124
P CRD013 Cardiofaciocutaneous Syndrome 72 0.038
125
OBS002 Obsessive-Compulsive Disorder 72 0.038
126
HYP458 Hyper Ige Syndrome 71 0.038
127
P WGN002 Wegener's Granulomatosis 71 0.038
128
DBT011 Diabetic Retinopathy 70 0.038
129
P ANG001 Angelman Syndrome 70 0.038
130
SPS077 Sepsis 70 0.038
131
VSC007 Vascular Disease 70 0.038
132
ACN002 Acanthosis Nigricans 69 0.038
133
BRN024 Bronchitis 69 0.038
134
ADN001 Adenosine Deaminase Deficiency 69 0.038
135
TRC008 Trachoma 68 0.038
136
c HPT016 Hepatitis B 68 0.038
137
P AMY004 Amyloidosis 67 0.038
138
ART021 Arteriosclerosis 67 0.038
139
P DGR001 Digeorge Syndrome 67 0.038
140
c NPH012 Nephrotic Syndrome 66 0.038
141
P PLY011 Polycystic Ovary Syndrome 66 0.038
142
OVR029 Ovarian Hyperstimulation Syndrome 66 0.038
143
GST009 Gastroschisis 66 0.038
144
P PRD008 Periodontitis 66 0.038
145
P HPT001 Hepatitis C 66 0.038
146
c AXN002 Axenfeld-Rieger Syndrome 66 0.038
147
SHG001 Shigellosis 65 0.038
148
P OVR049 Ovarian Disease 65 0.038
149
STT001 Status Epilepticus 65 0.038
150
P MCL015 Mucolipidosis Ii 64 0.038
151
ECL001 Eclampsia 64 0.038
152
ART019 Aortic Valve Stenosis 64 0.038
153
STF001 Stiff-Person Syndrome 63 0.038
154
c GLL020 Gallbladder Disease 63 0.038
155
HYP056 Hypoglycemia 63 0.038
156
CMP002 Campylobacteriosis 63 0.038
157
CYS005 Cysticercosis 63 0.038
158
CHG001 Chagas Disease 62 0.038
159
HYP066 Hyperglycemia 62 0.038
160
c HYP076 Hyperthyroidism 62 0.038
161
CRY003 Cryptosporidiosis 62 0.038
162
BTN003 Biotinidase Deficiency 62 0.038
163
GNG013 Gingivitis 62 0.038
164
P HRD011 Hereditary Spherocytosis 62 0.038
165
RBS003 Rabson-Mendenhall Syndrome 62 0.038
166
MYL020 Myelomeningocele 61 0.038
167
HV1006 Hiv-1 61 0.038
168
P CND004 Candidiasis 61 0.038
169
PLM001 Pulmonary Tuberculosis 60 0.038
170
TYP007 Typhoid Fever 60 0.038
171
c FML012 Familial Partial Lipodystrophy 59 0.038
172
LPD010 Lipodystrophy 59 0.038
173
MGC001 Megacolon 59 0.038
174
CHL014 Cholera 59 0.038
175
SCB001 Scabies 59 0.038
176
P INT068 Intestinal Disease 58 0.038
177
P TRN001 Transthyretin Amyloidosis 58 0.038
178
BLM002 Bulimia Nervosa 58 0.038
179
P CNG401 Congenital Heart Disease 58 0.038
180
BCT004 Bacteriuria 58 0.038
181
GLC003 Glucose Intolerance 58 0.038
182
HYP266 Hypoxia 57 0.038
183
SDR002 Siderosis 56 0.038
184
P MTB001 Metabolic Syndrome X 56 0.038
185
P RTN022 Retinal Vein Occlusion 56 0.038
186
c CNT016 Central Retinal Vein Occlusion 55 0.038
187
INS008 Insulin-Like Growth Factor I Deficiency 55 0.038
188
ACR005 Acrodermatitis 55 0.038
189
HMS001 Hemosiderosis 55 0.038
190
CRD005 Cardia Cancer 54 0.038
191
PRM003 Premature Ejaculation 54 0.038
192
SCR002 Scurvy 54 0.038
193
ART001 Arterial Tortuosity Syndrome 54 0.038
194
VND002 Van Der Woude Syndrome 54 0.038
195
SCH012 Schizoaffective Disorder 54 0.038
196
STT004 Steatorrhea 54 0.038
197
MCR010 Microcephaly 54 0.038
198
RTN023 Retinitis 53 0.038
199
P MSC003 Muscular Atrophy 53 0.038
200
c ACR001 Aicardi-Goutieres Syndrome 53 0.038
201
GST045 Gastroenteritis 53 0.038
202
AND003 Andersen-Tawil Syndrome 53 0.038
203
YLL001 Yellow Nail Syndrome 52 0.038
204
P HYP083 Hypopituitarism 52 0.038
205
AMY053 Amyloidosis, Secondary 52 0.038
206
NM001 Noma 52 0.038
207
c CNG012 Congenital Generalized Lipodystrophy 52 0.038
208
P PRP023 Peripheral Neuropathy 52 0.038
209
ESN005 Eosinophilic Gastroenteritis 52 0.038
210
THR013 Thoracic Outlet Syndrome 52 0.038
211
GLS007 Glossitis 51 0.038
212
IMP004 Impetigo 51 0.038
213
SHR001 Short Bowel Syndrome 51 0.038
214
P ALC004 Alcohol Abuse 51 0.038
215
LPD004 Lipoid Nephrosis 51 0.038
216
P CST002 Castleman's Disease 50 0.038
217
END072 Endotheliitis 50 0.038
218
c TCL004 T-Cell Leukemia 50 0.038
219
ONC002 Onchocerciasis 50 0.038
220
c BCT007 Bacterial Meningitis 49 0.038
221
MCR020 Microsporidiosis 49 0.038
222
HYP077 Hypertrichosis 49 0.038
223
ATX019 Ataxia with Vitamin E Deficiency 49 0.038
224
EXC002 Exocrine Pancreatic Insufficiency 49 0.038
225
ALC010 Alcoholic Cardiomyopathy 48 0.038
226
SVR005 Severe Pre-Eclampsia 47 0.038
227
MCR094 Microvillus Inclusion Disease 47 0.038
228
CNT025 Central Pontine Myelinolysis 46 0.038
229
TRN022 Transcobalamin Ii Deficiency 45 0.038
230
BNF002 Bone Fracture 45 0.038
231
MCR017 Macrocytic Anemia 45 0.038
232
FBR063 Fibrocalculous Pancreatic Diabetes 45 0.038
233
c FTL001 Fetal Alcohol Syndrome 45 0.038
234
LPT005 Leptin Deficiency 44 0.038
235
PLC005 Placental Insufficiency 43 0.038
236
FTT001 Fatty Liver Disease 43 0.038
237
AMN006 Aminoaciduria 43 0.038
238
HYP029 Hyperthyroxinemia 43 0.038
239
SNL007 Senile Cataract 43 0.038
240
RBF001 Riboflavin Deficiency 42 0.038
241
P ATX010 Ataxia Neuropathy Spectrum 41 0.038
242
5FL001 5-Fluorouracil Toxicity 41 0.038
243
ESP028 Esophageal Squamous Cell Carcinoma 40 0.038
244
HVD003 Hiv/aids 40 0.038
245
c HVY001 Heavy Chain Disease 39 0.038
246
WRN003 Wernicke Encephalopathy 39 0.038
247
c MLR021 Malaria, Severe 38 0.038
248
PLT008 Pili Torti 38 0.038
249
P WLM008 Wilms Tumor, Type 1 38 0.038
250
SPR066 Superficial Siderosis 38 0.038
251
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 37 0.038
252
IPX001 Ipex Syndrome 37 0.038
253
NRT005 North Carolina Macular Dystrophy 36 0.038
254
VRL011 Viral Infectious Disease 36 0.038
255
DYS070 Dysalbuminemic Hyperthyroxinemia 35 0.038
256
c HYP290 Hypobetalipoproteinemia, Familial, 2 35 0.038
257
SML020 Small Patella Syndrome 35 0.038
258
PYR016 Pyridoxine Deficiency 34 0.038
259
VSC044 Visceral Myopathy 32 0.038
260
SYN053 Syndromic Diarrhea 32 0.038
261
CNG127 Congenital Sucrase-Isomaltase Deficiency 31 0.038
262
c ALP060 Alpha Heavy-Chain Disease 29 0.038
263
c ATS059 Autosomal Dominant Hyper Ige Syndrome 29 0.038
264
PSD029 Pseudocholinesterase Deficiency 29 0.038
265
ARB001 Ariboflavinosis 28 0.038
266
ANK010 Ankylostomiasis 28 0.038
267
TNS007 Taeniasis 28 0.038
268
TFT003 Tufting Enteropathy 28 0.038
269
PYR004 Pyuria 28 0.038
270
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.038
271
ECT004 Ecthyma 27 0.038
272
HNM002 Hinman Syndrome 27 0.038
273
IRN002 Iron Metabolism Disease 26 0.038
274
MNT002 Mental Depression 23 0.038
275
ATR073 Atrophic Glossitis 23 0.038
276
c BNG076 Benign Exophthalmos Syndrome 22 0.038
277
BRL001 Brill-Zinsser Disease 19 0.038
278
HYP081 Hypolipoproteinemia 18 0.038
279
HYP481 Hyperbiliverdinemia 15 0.038