Search results for Ferrous gluconate

203 hits were found for Ferrous gluconate

# Family MCID Name MIFTS Score
1
IRN002 Iron Metabolism Disease 57 0.589
2
DFC004 Deficiency Anemia 75 0.506
3
IRN001 Iron Deficiency Anemia 58 0.426
4
NTR005 Nutritional Deficiency Disease 61 0.257
5
P KDN018 Kidney Disease 70 0.203
6
c CHR684 Chronic Kidney Disease 66 0.193
7
CNS004 Constipation 57 0.180
8
P DRR001 Diarrhea 57 0.176
9
c RHB024 Rhabdomyosarcoma 2 65 0.167
10
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.151
11
P TRN020 Turner Syndrome 65 0.139
12
48X005 48,xyyy 39 0.134
13
END030 End Stage Renal Failure 58 0.134
14
DRM006 Dermatitis 61 0.122
15
P INF037 Inflammatory Bowel Disease 56 0.122
16
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.121
17
CHL079 Children's Interstitial Lung Disease 27 0.117
18
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.117
19
ATX019 Ataxia with Vitamin E Deficiency 48 0.114
20
ADL002 Adult Syndrome 69 0.109
21
MLR004 Malaria 80 0.105
22
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.105
23
ALL026 Allergic Hypersensitivity Disease 64 0.103
24
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.102
25
c FNC043 Fanconi Anemia, Complementation Group E 62 0.102
26
HYP266 Hypoxia 56 0.100
27
DWN001 Down Syndrome 70 0.100
28
HMN044 Human Immunodeficiency Virus Type 1 71 0.096
29
P CLR023 Colorectal Cancer 98 0.096
30
P HDC001 Headache 57 0.094
31
P HRT032 Heart Disease 75 0.093
32
ACQ007 Acquired Immunodeficiency Syndrome 60 0.093
33
HYP781 Hypoascorbemia 50 0.091
34
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.090
35
CYS001 Cystic Fibrosis 80 0.089
36
RCK004 Rickets 69 0.086
37
CNG034 Congestive Heart Failure 70 0.086
38
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.086
39
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.086
40
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.086
41
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.086
42
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.086
43
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.086
44
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.086
45
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.086
46
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.086
47
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.086
48
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.086
49
CLT003 Colitis 62 0.085
50
P PRP029 Porphyria 62 0.085
51
c CHR682 Chronic Bilirubin Encephalopathy 38 0.085
52
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.085
53
IMM167 Immune Deficiency Disease 78 0.085
54
LPT014 Leptin Deficiency or Dysfunction 73 0.080
55
GST050 Gastrointestinal System Disease 56 0.080
56
P BRS047 Breast Cancer 96 0.079
57
SCH014 Schistosomiasis 56 0.079
58
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.079
59
P PRP003 Porphyria Cutanea Tarda 67 0.077
60
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.077
61
P OST002 Osteoporosis 73 0.076
62
P ADN016 Adenocarcinoma 64 0.076
63
PLS007 Plasmodium Falciparum Malaria 52 0.076
64
PRT036 Peritonitis 65 0.075
65
HYP005 Hypokalemia 55 0.075
66
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.074
67
DYS073 Dysphagia 50 0.074
68
PLC008 Placenta Disease 49 0.074
69
ULC004 Ulcerative Colitis 73 0.072
70
c PRC016 Pre-Eclampsia 63 0.072
71
GLS018 Glass Syndrome 53 0.072
72
OST012 Osteoarthritis 78 0.072
73
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.072
74
P NRP001 Neuropathy 56 0.072
75
RRD056 Rare Disease in Surgical Orthopedic 28 0.071
76
P LYM118 Lymphoma 68 0.069
77
CNT047 Contact Dermatitis 57 0.069
78
P EXN002 Exanthem 57 0.069
79
BCT022 Bacterial Infectious Disease 56 0.069
80
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.069
81
LYM019 Lymphosarcoma 47 0.069
82
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.069
83
c HYP595 Hypertension, Essential 84 0.068
84
STR067 Stroke, Ischemic 80 0.068
85
CRB039 Cerebrovascular Disease 69 0.068
86
P DMN002 Dementia 67 0.068
87
KHL003 Kohlschutter-Tonz Syndrome 64 0.068
88
DPR016 Depression 63 0.068
89
c ANM036 Anemia, Sideroblastic, 1 57 0.068
90
MNT002 Mental Depression 57 0.068
91
OCL069 Ocular Motor Apraxia 51 0.068
92
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.068
93
49X006 49, Xxxxy Syndrome 41 0.068
94
c THR092 Thrombophilia Due to Thrombin Defect 73 0.067
95
GST033 Gestational Diabetes 57 0.067
96
c LRG017 Large Intestine Cancer 47 0.067
97
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.066
98
P CNR004 Cone-Rod Dystrophy 2 71 0.065
99
SKN016 Skin Disease 63 0.065
100
c PNS012 Paine Syndrome 61 0.065
101
STM007 Stomatitis 49 0.065
102
P LNG032 Lung Cancer 97 0.061
103
P INF032 Infertility 57 0.061
104
THR024 Thrombosis 56 0.061
105
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.061
106
CRV035 Cervical Cancer 76 0.060
107
ANX010 Anxiety 72 0.060
108
P OCL013 Oculodentodigital Dysplasia 69 0.060
109
LPD008 Lipid Metabolism Disorder 62 0.060
110
TRN015 Transient Cerebral Ischemia 62 0.060
111
VSC002 Vascular Dementia 57 0.060
112
P GST044 Gastritis 55 0.060
113
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.060
114
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.060
115
c MGR028 Migraine with or Without Aura 1 69 0.060
116
P ATS364 Autism 65 0.060
117
P DBT009 Diabetes Mellitus 64 0.060
118
P CRN300 Coronary Heart Disease 1 63 0.060
119
P LPS004 Lupus Erythematosus 61 0.060
120
LNG099 Lung Disease 61 0.060
121
ISC004 Ischemia 60 0.060
122
P CRD246 Cardiovascular System Disease 56 0.060
123
HMP009 Haemophilus Influenzae 42 0.060
124
HYP001 Hypochromic Microcytic Anemia 38 0.060
125
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 37 0.060
126
MLN008 Melanoma 69 0.056
127
P THR014 Thrombocytopenia 68 0.056
128
SKN019 Skin Melanoma 67 0.056
129
P MSC005 Muscular Dystrophy 66 0.056
130
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.056
131
DSS008 Disease of Mental Health 57 0.056
132
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.056
133
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.052
134
c SYS001 Systemic Lupus Erythematosus 86 0.052
135
P RHM011 Rheumatoid Arthritis 80 0.052
136
c SPN225 Spondyloarthropathy 1 73 0.052
137
P ART022 Arthritis 70 0.052
138
BRN024 Bronchitis 68 0.052
139
c ATS007 Autism Spectrum Disorder 67 0.052
140
PRT037 Pertussis 65 0.052
141
PSR001 Psoriatic Arthritis 62 0.052
142
FTT001 Fatty Liver Disease 61 0.052
143
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.052
144
PLM033 Pulmonary Embolism 59 0.052
145
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.052
146
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.052
147
TLN003 Telangiectasis 51 0.052
148
P ECL001 Eclampsia 51 0.052
149
SBC016 Subacute Delirium 44 0.052
150
GST020 Gastric Antral Vascular Ectasia 41 0.052
151
PSD088 Pseudobulbar Affect 36 0.052
152
MYL069 Myeloma, Multiple 85 0.050
153
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.050
154
P GRF003 Graft-Versus-Host Disease 71 0.050
155
PSY004 Psychotic Disorder 67 0.050
156
P CRN018 Coronary Artery Anomaly 63 0.050
157
HYP066 Hyperglycemia 61 0.050
158
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.050
159
BRN004 Brain Edema 55 0.050
160
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.050
161
P RCT021 Rectum Cancer 53 0.050
162
ART140 Arteries, Anomalies of 53 0.050
163
P SHR001 Short Bowel Syndrome 52 0.050
164
ACR041 Acromelic Frontonasal Dysostosis 52 0.050
165
PLS009 Plasma Cell Neoplasm 51 0.050
166
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.050
168
P PHC003 Pheochromocytoma 71 0.042
169
c HPT073 Hepatitis C Virus 70 0.042
170
P HPT021 Hepatitis 67 0.042
171
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.042
172
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.042
173
c DPH024 Diaphragmatic Hernia, Congenital 64 0.042
174
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.042
175
c HPT001 Hepatitis C 63 0.042
176
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.042
177
CHL068 Cholestasis 60 0.042
178
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.042
179
P SLP005 Sleep Disorder 59 0.042
180
THY029 Thyroid Carcinoma 59 0.042
181
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.042
182
c ACT071 Acute Kidney Failure 59 0.042
183
GST045 Gastroenteritis 59 0.042
184
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.042
185
P ALP008 Alopecia 56 0.042
186
ALL010 Allergic Contact Dermatitis 55 0.042
187
ACT058 Active Peptic Ulcer Disease 55 0.042
188
P HYP076 Hyperthyroidism 55 0.042
189
VTM027 Vitamin D-Dependent Rickets, Type 2a 55 0.042
190
P VNS003 Venous Insufficiency 55 0.042
191
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 53 0.042
192
GST023 Gastric Ulcer 53 0.042
193
P AST007 Astrocytoma 50 0.042
194
P CHR345 Chronic Pain 50 0.042
195
HYP017 Hypophosphatemia 49 0.042
196
IRR003 Irritant Dermatitis 47 0.042
197
ADR040 Adrenal Gland Pheochromocytoma 46 0.042
198
P HMR005 Hemorrhoid 46 0.042
199
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.042
200
c CPL013 Capillary Malformations, Congenital 40 0.042
201
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.042
202
c PRG106 Progressive Muscular Dystrophy 33 0.042
203
STN013 Stenotrophomonas Maltophilia Infection 25 0.042
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