Search results for Ferrous fumarate

259 hits were found for Ferrous fumarate

# Family MCID Name MIFTS Score
1
IRN002 Iron Metabolism Disease 57 0.576
2
DFC004 Deficiency Anemia 75 0.498
3
IRN001 Iron Deficiency Anemia 58 0.430
4
48X005 48,xyyy 39 0.304
5
NTR005 Nutritional Deficiency Disease 61 0.304
6
HMN044 Human Immunodeficiency Virus Type 1 71 0.290
7
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.272
8
P PSR002 Psoriasis 62 0.258
9
PST011 Pustulosis of Palm and Sole 52 0.258
10
P HPT021 Hepatitis 67 0.240
11
ADL002 Adult Syndrome 69 0.220
12
CNS004 Constipation 57 0.218
13
LNG099 Lung Disease 61 0.209
14
IMM167 Immune Deficiency Disease 78 0.208
15
ACQ007 Acquired Immunodeficiency Syndrome 60 0.207
16
DPR016 Depression 63 0.207
17
MNT002 Mental Depression 57 0.207
18
P DRR001 Diarrhea 57 0.206
19
c RHB024 Rhabdomyosarcoma 2 65 0.205
20
CHL079 Children's Interstitial Lung Disease 27 0.197
21
P KDN018 Kidney Disease 70 0.192
22
c CHR684 Chronic Kidney Disease 66 0.177
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.170
24
P TRN020 Turner Syndrome 65 0.154
25
HMS001 Hemosiderosis 54 0.145
26
P RRH023 Rare Hereditary Hemochromatosis 41 0.145
27
DRM006 Dermatitis 61 0.144
28
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.143
29
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.137
30
LMY002 Leiomyoma 50 0.134
31
P INF037 Inflammatory Bowel Disease 56 0.134
32
ANX010 Anxiety 72 0.133
33
ATX019 Ataxia with Vitamin E Deficiency 48 0.131
34
DWN001 Down Syndrome 70 0.129
35
HYP266 Hypoxia 56 0.124
36
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.123
37
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.121
38
BRN024 Bronchitis 68 0.118
39
ALL026 Allergic Hypersensitivity Disease 64 0.117
40
c PSR017 Psoriasis 2 52 0.117
41
c PSR023 Psoriasis 1 49 0.117
42
c PSR028 Psoriasis 7 39 0.117
43
c PSR032 Psoriasis 11 38 0.117
44
c PSR018 Psoriasis 13 38 0.117
45
49X006 49, Xxxxy Syndrome 41 0.115
46
P HDC001 Headache 57 0.115
47
MLR004 Malaria 80 0.111
48
LMY014 Leiomyoma, Uterine 56 0.109
49
MTH071 Methane Production 26 0.109
50
c HYP595 Hypertension, Essential 84 0.109
51
PSY004 Psychotic Disorder 67 0.105
52
RCK004 Rickets 69 0.104
53
HYP781 Hypoascorbemia 50 0.103
54
c FNC043 Fanconi Anemia, Complementation Group E 62 0.103
55
P CRD246 Cardiovascular System Disease 56 0.103
56
END030 End Stage Renal Failure 58 0.099
57
HLC007 Helicobacter Pylori Infection 59 0.098
58
STR067 Stroke, Ischemic 80 0.097
59
CRB039 Cerebrovascular Disease 69 0.097
60
CNT047 Contact Dermatitis 57 0.095
61
P CLR023 Colorectal Cancer 98 0.094
62
CLT003 Colitis 62 0.094
63
c CHR682 Chronic Bilirubin Encephalopathy 38 0.094
64
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.094
65
P HRT032 Heart Disease 75 0.094
66
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.093
67
c PRC016 Pre-Eclampsia 63 0.093
68
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.093
69
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.093
70
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.093
71
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.093
72
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.093
73
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.093
74
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.093
75
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.093
76
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.093
77
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.093
78
c HPT001 Hepatitis C 63 0.093
79
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.091
80
CRH001 Crohn's Disease 74 0.090
81
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.090
82
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.090
83
HYP005 Hypokalemia 55 0.089
84
MYF001 Myofibroma 42 0.089
85
c HPT073 Hepatitis C Virus 70 0.088
86
SKN016 Skin Disease 63 0.088
87
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.088
88
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.088
89
LPT014 Leptin Deficiency or Dysfunction 73 0.087
90
c THR092 Thrombophilia Due to Thrombin Defect 73 0.087
91
CNG034 Congestive Heart Failure 70 0.086
92
P LPS004 Lupus Erythematosus 61 0.086
93
PCD001 Pica Disease 37 0.085
94
CYS001 Cystic Fibrosis 80 0.083
95
DYS073 Dysphagia 50 0.083
96
PLC008 Placenta Disease 49 0.083
97
P ART022 Arthritis 70 0.083
98
PSR001 Psoriatic Arthritis 62 0.083
99
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.083
100
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.081
101
P OCL013 Oculodentodigital Dysplasia 69 0.081
102
P DMN002 Dementia 67 0.081
103
KHL003 Kohlschutter-Tonz Syndrome 64 0.081
104
LPD008 Lipid Metabolism Disorder 62 0.081
105
c SYS001 Systemic Lupus Erythematosus 86 0.080
106
P DBT009 Diabetes Mellitus 64 0.080
107
P HYP086 Hypothyroidism 68 0.079
108
GST050 Gastrointestinal System Disease 56 0.079
109
GLS018 Glass Syndrome 53 0.079
110
CRH005 Crohn's Colitis 52 0.079
111
HLX001 Helix Syndrome 47 0.079
112
ANC001 Ancylostomiasis 39 0.079
113
P OST002 Osteoporosis 73 0.079
114
P EXN002 Exanthem 57 0.079
115
DSS008 Disease of Mental Health 57 0.079
116
P NRP001 Neuropathy 56 0.079
117
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.079
118
HYP017 Hypophosphatemia 49 0.079
119
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.079
120
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.079
121
VSC002 Vascular Dementia 57 0.077
122
P RHM011 Rheumatoid Arthritis 80 0.077
123
P CRN300 Coronary Heart Disease 1 63 0.077
124
ISC004 Ischemia 60 0.077
125
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.077
126
P CNR004 Cone-Rod Dystrophy 2 71 0.076
127
P SLP005 Sleep Disorder 59 0.076
128
ALL010 Allergic Contact Dermatitis 55 0.076
129
GST033 Gestational Diabetes 57 0.073
130
c LRG017 Large Intestine Cancer 47 0.073
131
P BRS047 Breast Cancer 96 0.073
132
TBC004 Tobacco Addiction 64 0.073
133
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.073
134
SBC016 Subacute Delirium 44 0.073
135
c SYS043 Systemic Lupus Erythematosus 1 38 0.073
136
P OVR042 Ovarian Cancer 89 0.072
137
c HMP029 Hemophilia a 65 0.072
138
OCL069 Ocular Motor Apraxia 51 0.072
139
c OVR114 Ovarian Cancer 1 38 0.072
140
P INT068 Intestinal Disease 52 0.072
141
c ACT071 Acute Kidney Failure 59 0.070
142
BRN004 Brain Edema 55 0.070
143
HMP009 Haemophilus Influenzae 42 0.069
144
PSD088 Pseudobulbar Affect 36 0.069
145
CRV035 Cervical Cancer 76 0.067
146
P NRB001 Neuroblastoma 71 0.067
147
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.066
148
P PHC003 Pheochromocytoma 71 0.066
149
P LYM118 Lymphoma 68 0.066
150
P CRN018 Coronary Artery Anomaly 63 0.066
151
c VRL010 Viral Hepatitis 51 0.066
152
LYM019 Lymphosarcoma 47 0.066
153
P RST001 Restless Legs Syndrome 54 0.066
154
c RST012 Restless Legs Syndrome 1 34 0.066
155
c SPN225 Spondyloarthropathy 1 73 0.064
156
P ATS364 Autism 65 0.064
157
PLM033 Pulmonary Embolism 59 0.064
158
P ECL001 Eclampsia 51 0.064
159
P SCK005 Sickle Cell Disease 50 0.064
160
P PRC031 Preeclampsia/eclampsia 1 37 0.064
161
OST012 Osteoarthritis 78 0.063
162
ADR040 Adrenal Gland Pheochromocytoma 46 0.063
163
P GST044 Gastritis 55 0.060
164
KRT002 Keratomalacia 48 0.060
165
c MGR028 Migraine with or Without Aura 1 69 0.059
166
P CRN037 Craniosynostosis 68 0.059
167
P INT143 Interstitial Cystitis 61 0.059
168
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.059
169
PRS034 Parasitic Helminthiasis Infectious Disease 49 0.059
170
HYP043 Hyperandrogenism 48 0.059
171
c CRN278 Craniosynostosis 1 45 0.059
172
OVR094 Ovarian Epithelial Cancer 38 0.059
173
c PLY105 Polycystic Ovary Syndrome 1 38 0.059
174
ISL062 Isolated Plagiocephaly 35 0.059
175
P ADN016 Adenocarcinoma 64 0.059
176
DPH001 Diphtheria 60 0.059
177
THR024 Thrombosis 56 0.059
178
ART140 Arteries, Anomalies of 53 0.059
179
SLP001 Sleeping Sickness 48 0.059
180
P GRF003 Graft-Versus-Host Disease 71 0.054
181
HYP056 Hypoglycemia 66 0.054
182
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.054
183
IRR002 Irritable Bowel Syndrome 63 0.054
184
HYP066 Hyperglycemia 61 0.054
185
c PNS012 Paine Syndrome 61 0.054
186
ADN018 Adenoma 58 0.054
187
BCT022 Bacterial Infectious Disease 56 0.054
188
P ALP008 Alopecia 56 0.054
189
ACR041 Acromelic Frontonasal Dysostosis 52 0.054
190
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.054
191
CHR178 Chromosomal Triplication 35 0.054
192
c HMC039 Hemochromatosis, Type 1 74 0.052
193
OTT002 Otitis Media 71 0.052
194
c ATS007 Autism Spectrum Disorder 67 0.052
195
FTT001 Fatty Liver Disease 61 0.052
196
P PLY011 Polycystic Ovary Syndrome 56 0.052
197
HMG005 Hemoglobinopathy 55 0.052
198
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.052
199
TLN003 Telangiectasis 51 0.052
200
PST021 Postpartum Depression 50 0.052
201
P LNG032 Lung Cancer 97 0.049
202
IDP011 Idiopathic Interstitial Pneumonia 63 0.049
203
P HML002 Hemolytic Anemia 62 0.049
204
P PLM036 Pulmonary Fibrosis 61 0.049
205
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.049
206
P CYS018 Cystitis 59 0.049
207
PPT005 Peptic Ulcer Disease 58 0.049
208
P INF032 Infertility 57 0.049
209
P PLY018 Polycythemia 55 0.049
210
GLC003 Glucose Intolerance 54 0.049
211
CLF001 Cleft Lip 53 0.049
212
TRY001 Trypanosomiasis 50 0.049
213
P CHR345 Chronic Pain 50 0.049
214
c INH020 Inherited Metabolic Disorder 46 0.049
215
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.049
216
PST092 Posttransplant Acute Limbic Encephalitis 29 0.049
217
MYL069 Myeloma, Multiple 85 0.042
218
P GST053 Gastric Cancer 83 0.042
219
PLM001 Pulmonary Tuberculosis 70 0.042
220
c PRM196 Premature Ovarian Failure 1 68 0.042
221
P THR014 Thrombocytopenia 68 0.042
222
P SKN015 Skin Carcinoma 67 0.042
223
P MSC005 Muscular Dystrophy 66 0.042
224
MSM014 Mismatch Repair Cancer Syndrome 65 0.042
225
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.042
226
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.042
227
P END044 Endometriosis 62 0.042
228
HYD038 Hydrops Fetalis, Nonimmune 61 0.042
229
GST045 Gastroenteritis 59 0.042
230
P PRV006 Pervasive Developmental Disorder 57 0.042
231
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.042
232
P FBR017 Fibrosarcoma 56 0.042
233
P MTC069 Mitochondrial Disorders 56 0.042
234
CLF004 Cleft Lip/palate 54 0.042
235
PRT038 Protein-Energy Malnutrition 54 0.042
236
PTT009 Pituitary Gland Disease 54 0.042
237
ACD008 Acid-Labile Subunit Deficiency 54 0.042
238
GST023 Gastric Ulcer 53 0.042
239
c MCR113 Microvascular Complications of Diabetes 3 52 0.042
240
PLS009 Plasma Cell Neoplasm 51 0.042
241
BWN001 Bowen-Conradi Syndrome 51 0.042
242
STM007 Stomatitis 49 0.042
243
PNN001 Panniculitis 49 0.042
244
VCC001 Vaccinia 49 0.042
245
P GND004 Gonadal Dysgenesis 49 0.042
246
CLN045 Colonic Benign Neoplasm 49 0.042
247
INT078 Intracranial Thrombosis 48 0.042
248
IRR003 Irritant Dermatitis 47 0.042
249
c MCR120 Microvascular Complications of Diabetes 7 47 0.042
250
P PRP056 Porphyria, Acute Hepatic 46 0.042
251
PPL001 Papillary Adenoma 45 0.042
252
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.042
253
PRM013 Premature Menopause 42 0.042
254
c MCR130 Microvascular Complications of Diabetes 6 41 0.042
255
c MCR133 Microvascular Complications of Diabetes 4 41 0.042
256
c LYM150 Lymphatic Malformation 7 41 0.042
257
c CPL013 Capillary Malformations, Congenital 40 0.042
258
INT076 Intracranial Sinus Thrombosis 32 0.042
259
MLR020 Malaria, Mild 28 0.042
Content
Loading form....