Search results for Fe2+

314 hits were found for Fe2+

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.983
2
HMS001 Hemosiderosis 48 2.836
3
P RRH023 Rare Hereditary Hemochromatosis 53 2.829
4
IRN002 Iron Metabolism Disease 56 2.646
5
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.824
6
c PLM128 Pulmonary Hypertension, Primary, 2 28 1.547
7
P PRP029 Porphyria 60 1.542
8
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.528
9
DPH001 Diphtheria 59 1.528
10
DFC004 Deficiency Anemia 74 1.479
11
P PNM006 Pneumoconiosis 55 1.450
12
ANT018 Anthracosis 51 1.450
13
MTH071 Methane Production 25 1.449
14
IRN001 Iron Deficiency Anemia 58 1.415
15
c HMC039 Hemochromatosis, Type 1 73 1.414
16
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.414
17
P ALZ034 Alzheimer Disease 87 1.356
18
P THL005 Thalassemia 56 1.286
19
P MYC084 Mycobacterium Tuberculosis 1 68 1.259
20
c ACT071 Acute Kidney Failure 60 1.241
21
48X005 48,xyyy 39 1.128
22
HYP266 Hypoxia 56 1.110
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.025
24
PRP083 Porphyria, Acute Intermittent 64 1.000
25
c RNG023 Ring Chromosome 7 43 1.000
26
P BRS047 Breast Cancer 97 0.973
27
HLX001 Helix Syndrome 47 0.943
28
P ANP001 Anaplastic Large Cell Lymphoma 61 0.943
29
c BTT014 Beta-Thalassemia 72 0.943
30
ACT078 Acute Porphyria 50 0.943
31
P VNS003 Venous Insufficiency 54 0.910
32
P PRK057 Parkinson Disease, Late-Onset 79 0.910
33
ALC007 Alcohol Dependence 65 0.910
34
BLC012 Bile Acid Malabsorption, Primary 43 0.910
35
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.910
36
HYP066 Hyperglycemia 60 0.910
37
CNS004 Constipation 56 0.910
38
ELS001 Eales Disease 45 0.910
39
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 0.910
40
P HNT016 Huntington Disease 73 0.869
41
HND015 Hand Skill, Relative 29 0.869
42
BRN071 Brain Injury 50 0.869
43
CRV035 Cervical Cancer 72 0.817
44
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.817
45
P LNG032 Lung Cancer 98 0.817
46
P LTR001 Lateral Sclerosis 58 0.817
47
P GRF003 Graft-Versus-Host Disease 71 0.691
48
MLR004 Malaria 78 0.691
49
KLB003 Klebsiella Pneumonia 49 0.691
50
P NRB001 Neuroblastoma 66 0.565
51
ADR040 Adrenal Gland Pheochromocytoma 45 0.473
52
P PHC003 Pheochromocytoma 70 0.473
53
ANX004 Anoxia 40 0.455
54
P MTH007 Methemoglobinemia 46 0.419
55
LYS002 Lysosomal Storage Disease 51 0.399
56
47X002 47,xyy 48 0.399
57
c MCL013 Mucolipidosis Iv 64 0.379
58
P MCL001 Mucolipidosis 49 0.379
59
c HNT011 Huntington Disease-Like 3 33 0.379
60
PPL052 Papillomatosis, Confluent and Reticulated 34 0.379
61
P PRP003 Porphyria Cutanea Tarda 66 0.379
62
THY123 Thyroid Gland Follicular Carcinoma 53 0.379
63
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.379
64
THY029 Thyroid Carcinoma 54 0.379
65
c FBR075 Febrile Seizures, Familial, 2 32 0.357
66
ORL011 Oral Cancer 60 0.357
67
P PRK039 Parkinsonism 55 0.334
68
P FRD001 Friedreich Ataxia 62 0.334
69
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 22 0.309
70
P KLZ004 Kala-Azar 1 41 0.309
71
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.309
72
DYS015 Dysentery 50 0.309
73
P VSC007 Vascular Disease 62 0.309
74
P SDR002 Siderosis 42 0.309
75
LSH001 Leishmaniasis 63 0.309
76
INS024 Insulin-Like Growth Factor I 77 0.282
77
c PRC016 Pre-Eclampsia 64 0.282
78
c ATR087 Atrial Standstill 1 74 0.282
79
HYP781 Hypoascorbemia 52 0.282
80
P CRD119 Cardiac Arrest 68 0.282
81
P ALC033 Alcohol Use Disorder 67 0.282
82
IMP005 Impotence 52 0.282
83
TXC005 Toxic Shock Syndrome 62 0.282
84
P PLM036 Pulmonary Fibrosis 65 0.282
85
P CHR012 Chronic Granulomatous Disease 69 0.282
86
AGN016 Aging 54 0.253
87
c HNT004 Huntington Disease-Like 2 51 0.253
88
P OST002 Osteoporosis 77 0.253
89
P LPR021 Leprosy 3 71 0.253
90
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.253
91
c HYP836 Hypercholesterolemia, Familial, 1 73 0.253
92
CYN002 Cyanosis, Transient Neonatal 43 0.253
93
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.253
94
URM002 Uremia 47 0.253
95
TTN003 Tetanus 64 0.253
96
GLM045 Glioma 62 0.253
97
GLL048 Glial Tumor 52 0.253
98
P PRC019 Precocious Puberty 49 0.253
99
HNS001 Hansen's Disease 32 0.253
100
c TYP009 Type 2 Diabetes Mellitus 92 0.219
101
DWN001 Down Syndrome 70 0.219
103
P STR022 Stargardt Disease 61 0.219
104
P HYP730 Hypogonadotropic Hypogonadism 54 0.219
105
PMP014 Pemphigoid 49 0.219
106
c TYP008 Type 1 Diabetes Mellitus 77 0.219
107
HYP784 Hypogonadism, Male 43 0.219
108
c STR084 Stargardt Disease 1 53 0.219
109
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.219
110
HRW001 Hair Whorl 35 0.219
111
P EPL164 Epilepsy 70 0.219
112
P UVT001 Uveitis 57 0.219
113
CRB039 Cerebrovascular Disease 65 0.219
114
P OVR046 Ovarian Cyst 44 0.219
115
HYP080 Hypogonadism 49 0.219
116
AMN001 Amenorrhea 53 0.219
117
CHL123 Chlamydia 58 0.219
118
FCL014 Focal Epilepsy 53 0.219
119
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.219
120
GST045 Gastroenteritis 58 0.219
121
SRF006 Surfactant Dysfunction 33 0.219
122
CNG562 Congenital Hypogonadotropic Hypogonadism 28 0.219
123
PYR009 Pyridoxine Deficiency Anemia 35 0.219
124
LNG099 Lung Disease 62 0.219
125
BLL006 Bullous Pemphigoid 61 0.219
126
SPN186 Spinal Cord Injury 61 0.219
127
P RTN016 Retinal Degeneration 52 0.219
128
P MSC005 Muscular Dystrophy 66 0.219
129
PST092 Posttransplant Acute Limbic Encephalitis 29 0.219
130
c ACT134 Acute Liver Failure 57 0.219
131
c ALT008 Alternating Hemiplegia of Childhood 1 39 0.179
132
ESP021 Esophageal Cancer 84 0.179
133
OCL069 Ocular Motor Apraxia 57 0.179
134
c MCR133 Microvascular Complications of Diabetes 4 41 0.179
135
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.179
136
MYL009 Myelodysplastic Syndrome 67 0.179
137
HYP001 Hypochromic Microcytic Anemia 36 0.179
138
ATS010 Autosomal Recessive Disease 42 0.179
139
DSS032 Disease by Infectious Agent 55 0.179
140
MLD018 Mild Cognitive Impairment 48 0.179
141
BNR002 Bone Resorption Disease 47 0.179
142
URL001 Urolithiasis 45 0.179
143
MDD018 Middle East Respiratory Syndrome 44 0.179
144
STR103 Streptococcus Pneumonia 47 0.179
145
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.179
146
FNG015 Fingers, Relative Length of 12 0.179
147
c SYS001 Systemic Lupus Erythematosus 86 0.179
148
c MCR113 Microvascular Complications of Diabetes 3 52 0.179
149
c MCR130 Microvascular Complications of Diabetes 6 41 0.179
150
c MCR120 Microvascular Complications of Diabetes 7 47 0.179
151
CHR100 Chronic Ulcer of Skin 57 0.179
152
ISC004 Ischemia 61 0.179
153
c ACT027 Acute Pancreatitis 60 0.179
154
BRN004 Brain Edema 54 0.179
155
LVR012 Liver Cirrhosis 62 0.179
156
P PNC044 Pancreatitis 61 0.179
157
PTT009 Pituitary Gland Disease 53 0.179
158
EXT007 Extracutaneous Mastocytoma 38 0.179
159
PRT037 Pertussis 49 0.179
160
P GCH001 Gaucher's Disease 69 0.179
161
DMP001 Dumping Syndrome 43 0.179
162
c DLT002 Dilated Cardiomyopathy 79 0.179
163
DSS009 Disseminated Intravascular Coagulation 56 0.179
164
MST004 Mast Cell Neoplasm 41 0.179
165
P ART023 Arthropathy 60 0.179
166
P ART021 Arteriosclerosis 53 0.179
167
P BNG032 Benign Mesothelioma 53 0.179
168
PLG002 Plague 58 0.179
169
P GLL018 Gallbladder Cancer 53 0.179
170
OST159 Osteogenic Sarcoma 66 0.179
171
STN013 Stenotrophomonas Maltophilia Infection 26 0.179
172
P HRP006 Herpes Simplex 65 0.179
173
P SDR003 Sideroblastic Anemia 49 0.179
174
P MYP004 Myopathy 67 0.179
175
HYP005 Hypokalemia 55 0.179
176
P INF038 Influenza 68 0.179
177
P ART022 Arthritis 70 0.179
178
PPT005 Peptic Ulcer Disease 58 0.179
179
P LPS004 Lupus Erythematosus 61 0.179
180
P AMY004 Amyloidosis 69 0.179
181
P DBT009 Diabetes Mellitus 67 0.179
182
HMG009 Hemoglobin Zurich 21 0.179
183
HMP009 Haemophilus Influenzae 41 0.179
184
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.179
185
P TXP001 Toxoplasmosis 60 0.179
186
PRX001 Peroxisomal Disease 46 0.179
187
P TYR004 Tyrosinemia 49 0.179
188
c ACQ047 Acquired Methemoglobinemia 30 0.179
189
P BLD134 Bladder Cancer 79 0.126
190
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.126
191
P PRS040 Prostate Cancer 95 0.126
192
CPR004 Coproporphyria, Hereditary 57 0.126
193
LYM133 Lymphoma, Hodgkin, Classic 74 0.126
194
HLC007 Helicobacter Pylori Infection 67 0.126
195
RFS006 Refsum Disease, Classic 63 0.126
196
HMC014 Homocysteinemia 52 0.126
197
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.126
198
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.126
199
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 54 0.126
200
WST005 West Nile Virus 55 0.126
201
c BRS111 Breast-Ovarian Cancer, Familial 2 54 0.126
202
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.126
203
P INF037 Inflammatory Bowel Disease 53 0.126
204
P FML340 Familial Episodic Pain Syndrome 50 0.126
205
P PLY041 Polymyositis 59 0.126
206
P DRM010 Dermatomyositis 61 0.126
207
P RNL015 Renal Hypertension 45 0.126
208
P PTY003 Pityriasis Rubra Pilaris 57 0.126
209
ATH013 Atherosclerosis Susceptibility 63 0.126
210
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.126
211
FCS014 Fucosidase Regulator 15 0.126
212
c FNC027 Fanconi Anemia, Complementation Group a 81 0.126
213
c DWL002 Dowling-Degos Disease 1 58 0.126
214
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.126
215
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.126
216
ORL015 Oral Squamous Cell Carcinoma 43 0.126
217
MTL005 Metal Allergy 39 0.126
218
CRH005 Crohn's Colitis 53 0.126
219
HYP859 Hypotonia, Hypoventilation, Impaired Intellectual Development, Dysautonomia, Epilepsy, and Eye Abnormalities 27 0.126
220
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.126
221
ACR006 Aceruloplasminemia 63 0.126
222
c HPT073 Hepatitis C Virus 71 0.126
223
P HYP750 Hypertriglyceridemia, Familial 62 0.126
224
c EXD008 Exudative Vitreoretinopathy 1 71 0.126
225
PFF001 Pfeiffer Syndrome 77 0.126
226
PLT031 Platelet Membrane Fluidity 28 0.126
227
PRR015 Preauricular Fistulae, Congenital 19 0.126
228
c RTN142 Retinitis Pigmentosa 38 39 0.126
229
P LNG064 Lung Cancer Susceptibility 3 70 0.126
230
TTT001 Tatton-Brown-Rahman Syndrome 45 0.126
231
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.126
232
SMT004 Smith-Lemli-Opitz Syndrome 69 0.126
233
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 46 0.126
234
MCR018 Microcytic Anemia 47 0.126
235
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.126
236
IRN004 Iron-Refractory Iron Deficiency Anemia 46 0.126
237
KRT019 Keratitis, Hereditary 66 0.126
238
PRP027 Peripheral Vascular Disease 71 0.126
239
P PLY019 Polyneuropathy 53 0.126
240
CHL014 Cholera 62 0.126
241
CRT013 Carotid Stenosis 51 0.126
242
c SVR005 Severe Pre-Eclampsia 50 0.126
243
P DRR001 Diarrhea 55 0.126
244
CHL068 Cholestasis 61 0.126
245
GLB002 Glioblastoma 67 0.126
246
CNT047 Contact Dermatitis 57 0.126
247
HRY003 Hairy Cell Leukemia 61 0.126
248
P PRM002 Primary Hyperoxaluria 65 0.126
249
P PRN023 Prion Disease 60 0.126
250
CLC001 Calciphylaxis 50 0.126
251
P CNJ013 Conjunctivitis 66 0.126
252
CNN005 Connective Tissue Disease 66 0.126
253
DNT012 Dental Caries 53 0.126
254
c HPT001 Hepatitis C 61 0.126
255
P HPT021 Hepatitis 68 0.126
256
ADN075 Adenomyoma 32 0.126
257
PPL022 Papilloma 53 0.126
258
P MLN008 Melanoma 75 0.126
259
P RCT021 Rectum Cancer 54 0.126
260
HYP014 Hyperuricemia 51 0.126
261
P KDN017 Kidney Cancer 60 0.126
262
P ECL001 Eclampsia 52 0.126
263
P CRD246 Cardiovascular System Disease 55 0.126
264
ADL030 Adult-Onset Still's Disease 59 0.126
265
P HYP086 Hypothyroidism 69 0.126
266
SQM002 Squamous Cell Papilloma 45 0.126
267
P DMN001 Diamond-Blackfan Anemia 73 0.126
268
URT001 Urethritis 52 0.126
269
CRY005 Cryptococcosis 61 0.126
270
GTR002 Goiter 52 0.126
271
P MLN007 Male Infertility 56 0.126
272
CHG001 Chagas Disease 65 0.126
273
GST023 Gastric Ulcer 52 0.126
274
ASB001 Asbestosis 47 0.126
275
P NPH012 Nephrotic Syndrome 62 0.126
276
P LKM002 Leukemia 66 0.126
277
P LCT001 Lactic Acidosis 50 0.126
278
P GLM007 Glomerulonephritis 59 0.126
279
NWC001 Newcastle Disease 48 0.126
280
P FBR017 Fibrosarcoma 55 0.126
281
P SKN015 Skin Carcinoma 71 0.126
282
VCC001 Vaccinia 49 0.126
283
TRN015 Transient Cerebral Ischemia 62 0.126
284
TRT001 Teratocarcinoma 41 0.126
285
EMB004 Embryonal Carcinoma 55 0.126
286
SKN020 Skin Papilloma 40 0.126
287
MSC157 Muscular Dystrophy, Duchenne Type 79 0.126
288
c LKM061 Leukemia, Acute Myeloid 83 0.126
289
P CRN300 Coronary Heart Disease 1 73 0.126
290
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.126
291
BNG036 Bone Giant Cell Tumor 48 0.126
292
P GST044 Gastritis 55 0.126
293
CRT033 Corticobasal Degeneration 48 0.126
294
CYT002 Cytokine Deficiency 43 0.126
295
LKP003 Leukoplakia 39 0.126
296
P ENC018 Encephalopathy 62 0.126
297
P TRM003 Tremor 50 0.126
298
P CTR002 Cataract 59 0.126
299
CRH001 Crohn's Disease 80 0.126
300
STM007 Stomatitis 52 0.126
301
SNL007 Senile Cataract 40 0.126
302
ORL006 Oral Mucosa Leukoplakia 22 0.126
303
P KDN018 Kidney Disease 72 0.126
304
SCR011 Scrapie 39 0.126
305
c RNG015 Ring Chromosome 2 22 0.126
306
CHR178 Chromosomal Triplication 34 0.126
307
ALL014 Allergic Encephalomyelitis 34 0.126
308
CRT015 Carotid Artery Occlusion 45 0.126
309
P HYP076 Hyperthyroidism 53 0.126
310
c FML324 Familial Porphyria Cutanea Tarda 29 0.126
311
FTT001 Fatty Liver Disease 61 0.126
312
HVY002 Heavy Metal Poisoning 22 0.126
313
ASB003 Asbestos Intoxication 32 0.126
314
ARG004 Argyria 26 0.126
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