Search results for Fe2+

311 hits were found for Fe2+

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.993
2
HMS001 Hemosiderosis 48 2.845
3
P RRH023 Rare Hereditary Hemochromatosis 52 2.838
4
IRN002 Iron Metabolism Disease 56 2.654
5
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.830
6
c PLM128 Pulmonary Hypertension, Primary, 2 28 1.552
7
P PRP029 Porphyria 60 1.547
8
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.532
9
DPH001 Diphtheria 59 1.532
10
ANT018 Anthracosis 50 1.454
11
P PNM006 Pneumoconiosis 55 1.454
12
DFC004 Deficiency Anemia 74 1.454
13
MTH071 Methane Production 24 1.454
14
IRN001 Iron Deficiency Anemia 58 1.420
15
c HMC039 Hemochromatosis, Type 1 73 1.419
16
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.419
17
P THL005 Thalassemia 56 1.290
18
P MYC084 Mycobacterium Tuberculosis 1 68 1.263
19
c ACT071 Acute Kidney Failure 60 1.245
20
48X005 48,xyyy 39 1.132
21
P ALZ034 Alzheimer Disease 87 1.073
22
HYP266 Hypoxia 56 1.073
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.028
24
PRP083 Porphyria, Acute Intermittent 64 1.003
25
c RNG023 Ring Chromosome 7 43 1.003
26
HLX001 Helix Syndrome 47 0.946
27
c BTT014 Beta-Thalassemia 72 0.946
28
P ANP001 Anaplastic Large Cell Lymphoma 59 0.946
29
ACT078 Acute Porphyria 50 0.946
30
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.912
31
ALC007 Alcohol Dependence 65 0.912
32
BLC012 Bile Acid Malabsorption, Primary 45 0.912
33
P PRK057 Parkinson Disease, Late-Onset 79 0.912
34
P VNS003 Venous Insufficiency 54 0.912
35
CNS004 Constipation 56 0.912
36
ELS001 Eales Disease 46 0.912
37
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 0.912
38
HND015 Hand Skill, Relative 29 0.872
39
P HNT016 Huntington Disease 73 0.872
40
HYP066 Hyperglycemia 60 0.872
41
P LNG032 Lung Cancer 98 0.820
42
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.820
43
CRV035 Cervical Cancer 72 0.820
44
P LTR001 Lateral Sclerosis 57 0.820
45
MLR004 Malaria 77 0.693
46
P GRF003 Graft-Versus-Host Disease 71 0.693
47
KLB003 Klebsiella Pneumonia 49 0.693
48
BRN071 Brain Injury 50 0.693
49
P NRB001 Neuroblastoma 66 0.552
50
P PHC003 Pheochromocytoma 70 0.474
51
ADR040 Adrenal Gland Pheochromocytoma 45 0.474
52
ANX004 Anoxia 40 0.457
53
P MTH007 Methemoglobinemia 46 0.420
54
LYS002 Lysosomal Storage Disease 51 0.401
55
c HNT011 Huntington Disease-Like 3 33 0.380
56
PPL052 Papillomatosis, Confluent and Reticulated 34 0.380
57
c MCL013 Mucolipidosis Iv 64 0.380
58
P PRP003 Porphyria Cutanea Tarda 66 0.380
59
P MCL001 Mucolipidosis 49 0.380
60
THY123 Thyroid Gland Follicular Carcinoma 53 0.380
61
47X002 47,xyy 47 0.380
62
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.380
63
THY029 Thyroid Carcinoma 55 0.380
64
c FBR075 Febrile Seizures, Familial, 2 32 0.358
65
ORL011 Oral Cancer 60 0.358
66
P FRD001 Friedreich Ataxia 62 0.335
67
P PRK039 Parkinsonism 55 0.335
68
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.310
69
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.310
70
P KLZ004 Kala-Azar 1 41 0.310
71
P SDR002 Siderosis 42 0.310
72
P VSC007 Vascular Disease 62 0.310
73
DYS015 Dysentery 49 0.310
74
LSH001 Leishmaniasis 63 0.310
75
P CRD119 Cardiac Arrest 68 0.283
76
INS024 Insulin-Like Growth Factor I 77 0.283
77
HYP781 Hypoascorbemia 52 0.283
78
c ATR087 Atrial Standstill 1 74 0.283
79
IMP005 Impotence 52 0.283
80
P ALC033 Alcohol Use Disorder 67 0.283
81
P PLM036 Pulmonary Fibrosis 65 0.283
82
P CHR012 Chronic Granulomatous Disease 69 0.283
83
c PRC016 Pre-Eclampsia 64 0.283
84
TXC005 Toxic Shock Syndrome 61 0.283
85
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.253
86
c HNT004 Huntington Disease-Like 2 51 0.253
87
P OST002 Osteoporosis 76 0.253
88
AGN016 Aging 53 0.253
89
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.253
90
CYN002 Cyanosis, Transient Neonatal 43 0.253
91
P LPR021 Leprosy 3 71 0.253
92
c HYP836 Hypercholesterolemia, Familial, 1 73 0.253
93
URM002 Uremia 47 0.253
94
TTN003 Tetanus 64 0.253
95
GLM045 Glioma 62 0.253
96
HNS001 Hansen's Disease 32 0.253
97
P PRC019 Precocious Puberty 48 0.253
98
GLL048 Glial Tumor 51 0.253
99
P STR022 Stargardt Disease 61 0.219
100
DWN001 Down Syndrome 70 0.219
101
c TYP009 Type 2 Diabetes Mellitus 91 0.219
102
HYP784 Hypogonadism, Male 43 0.219
103
c STR084 Stargardt Disease 1 54 0.219
105
c TYP008 Type 1 Diabetes Mellitus 77 0.219
106
HRW001 Hair Whorl 35 0.219
107
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.219
108
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.219
109
CHL123 Chlamydia 58 0.219
110
FCL014 Focal Epilepsy 53 0.219
111
HYP080 Hypogonadism 49 0.219
112
P HYP730 Hypogonadotropic Hypogonadism 57 0.219
113
GST045 Gastroenteritis 58 0.219
114
AMN001 Amenorrhea 53 0.219
115
P EPL164 Epilepsy 70 0.219
116
P UVT001 Uveitis 57 0.219
117
PMP014 Pemphigoid 48 0.219
118
BLL006 Bullous Pemphigoid 61 0.219
119
CRB039 Cerebrovascular Disease 65 0.219
120
P OVR046 Ovarian Cyst 43 0.219
121
PYR009 Pyridoxine Deficiency Anemia 35 0.219
122
P RTN016 Retinal Degeneration 52 0.219
123
LNG099 Lung Disease 62 0.219
124
P MSC005 Muscular Dystrophy 66 0.219
125
CNG562 Congenital Hypogonadotropic Hypogonadism 28 0.219
126
SRF006 Surfactant Dysfunction 33 0.219
127
SPN186 Spinal Cord Injury 60 0.219
128
PST092 Posttransplant Acute Limbic Encephalitis 29 0.219
129
c ACT134 Acute Liver Failure 57 0.219
130
MYL009 Myelodysplastic Syndrome 67 0.179
131
c SYS001 Systemic Lupus Erythematosus 85 0.179
132
FNG015 Fingers, Relative Length of 12 0.179
133
OST159 Osteogenic Sarcoma 66 0.179
134
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.179
135
CHR100 Chronic Ulcer of Skin 57 0.179
136
DSS032 Disease by Infectious Agent 55 0.179
137
ATS010 Autosomal Recessive Disease 42 0.179
138
c MCR133 Microvascular Complications of Diabetes 4 41 0.179
139
c MCR113 Microvascular Complications of Diabetes 3 52 0.179
140
c MCR130 Microvascular Complications of Diabetes 6 41 0.179
141
c MCR120 Microvascular Complications of Diabetes 7 47 0.179
142
HYP001 Hypochromic Microcytic Anemia 36 0.179
143
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.179
144
c ALT008 Alternating Hemiplegia of Childhood 1 39 0.179
145
ESP021 Esophageal Cancer 84 0.179
146
BNR002 Bone Resorption Disease 47 0.179
147
DSS009 Disseminated Intravascular Coagulation 56 0.179
148
MLD018 Mild Cognitive Impairment 48 0.179
149
P ART021 Arteriosclerosis 53 0.179
150
P GCH001 Gaucher's Disease 69 0.179
151
P BNG032 Benign Mesothelioma 53 0.179
152
STR103 Streptococcus Pneumonia 47 0.179
153
LVR012 Liver Cirrhosis 62 0.179
154
BRN004 Brain Edema 54 0.179
155
MST004 Mast Cell Neoplasm 41 0.179
156
P GLL018 Gallbladder Cancer 59 0.179
157
ISC004 Ischemia 61 0.179
158
PTT009 Pituitary Gland Disease 52 0.179
159
MDD018 Middle East Respiratory Syndrome 44 0.179
160
HYP005 Hypokalemia 55 0.179
161
P MYP004 Myopathy 67 0.179
162
P ART023 Arthropathy 59 0.179
163
EXT007 Extracutaneous Mastocytoma 38 0.179
164
P PNC044 Pancreatitis 61 0.179
165
c ACT027 Acute Pancreatitis 60 0.179
166
c DLT002 Dilated Cardiomyopathy 79 0.179
167
URL001 Urolithiasis 45 0.179
168
DMP001 Dumping Syndrome 43 0.179
169
PRT037 Pertussis 49 0.179
170
P CTR002 Cataract 59 0.179
171
PLG002 Plague 58 0.179
172
P TYR004 Tyrosinemia 49 0.179
173
PRX001 Peroxisomal Disease 46 0.179
174
P SDR003 Sideroblastic Anemia 49 0.179
175
PPT005 Peptic Ulcer Disease 58 0.179
176
P INF038 Influenza 68 0.179
177
P LPS004 Lupus Erythematosus 61 0.179
178
P TXP001 Toxoplasmosis 59 0.179
179
HMP009 Haemophilus Influenzae 41 0.179
180
STN013 Stenotrophomonas Maltophilia Infection 26 0.179
181
P HRP006 Herpes Simplex 65 0.179
182
P AMY004 Amyloidosis 69 0.179
183
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.179
184
HMG009 Hemoglobin Zurich 21 0.179
185
c ACQ047 Acquired Methemoglobinemia 30 0.179
186
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.127
187
P CRN300 Coronary Heart Disease 1 73 0.127
188
CRH005 Crohn's Colitis 53 0.127
189
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.127
190
ACR006 Aceruloplasminemia 63 0.127
191
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.127
192
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.127
193
ORL015 Oral Squamous Cell Carcinoma 43 0.127
194
P INF037 Inflammatory Bowel Disease 53 0.127
195
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.127
196
PFF001 Pfeiffer Syndrome 77 0.127
197
ATH013 Atherosclerosis Susceptibility 63 0.127
198
PRR015 Preauricular Fistulae, Congenital 20 0.127
199
c DWL002 Dowling-Degos Disease 1 58 0.127
200
LYM133 Lymphoma, Hodgkin, Classic 69 0.127
201
OCL069 Ocular Motor Apraxia 57 0.127
202
P PTY003 Pityriasis Rubra Pilaris 57 0.127
203
PLT031 Platelet Membrane Fluidity 28 0.127
204
CPR004 Coproporphyria, Hereditary 57 0.127
205
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.127
206
FCS014 Fucosidase Regulator 15 0.127
207
c FNC027 Fanconi Anemia, Complementation Group a 80 0.127
208
MSC157 Muscular Dystrophy, Duchenne Type 78 0.127
209
P BLD134 Bladder Cancer 79 0.127
210
RFS006 Refsum Disease, Classic 63 0.127
211
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.127
212
c EXD008 Exudative Vitreoretinopathy 1 71 0.127
213
c LKM061 Leukemia, Acute Myeloid 83 0.127
214
HMC014 Homocysteinemia 52 0.127
215
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.127
216
HYP859 Hypotonia, Hypoventilation, Impaired Intellectual Development, Dysautonomia, Epilepsy, and Eye Abnormalities 27 0.127
217
PRP027 Peripheral Vascular Disease 71 0.127
218
c HPT073 Hepatitis C Virus 70 0.127
219
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 47 0.127
220
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.127
221
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.127
222
IRN004 Iron-Refractory Iron Deficiency Anemia 46 0.127
223
KRT019 Keratitis, Hereditary 66 0.127
224
P HYP750 Hypertriglyceridemia, Familial 61 0.127
225
SMT004 Smith-Lemli-Opitz Syndrome 69 0.127
226
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.127
227
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.127
228
c RTN142 Retinitis Pigmentosa 38 39 0.127
229
TTT001 Tatton-Brown-Rahman Syndrome 44 0.127
230
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 54 0.127
231
WST005 West Nile Virus 55 0.127
232
HLC007 Helicobacter Pylori Infection 67 0.127
233
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.127
234
P LNG064 Lung Cancer Susceptibility 3 69 0.127
235
MTL005 Metal Allergy 40 0.127
236
P NPH012 Nephrotic Syndrome 61 0.127
237
P PLY041 Polymyositis 58 0.127
238
ASB001 Asbestosis 47 0.127
239
GST023 Gastric Ulcer 52 0.127
240
P RCT021 Rectum Cancer 54 0.127
241
P LKM002 Leukemia 65 0.127
242
DNT012 Dental Caries 53 0.127
243
VCC001 Vaccinia 49 0.127
244
P PRM002 Primary Hyperoxaluria 65 0.127
245
GLB002 Glioblastoma 67 0.127
246
ADN075 Adenomyoma 31 0.127
247
PPL022 Papilloma 53 0.127
248
CNT047 Contact Dermatitis 56 0.127
249
HRY003 Hairy Cell Leukemia 53 0.127
250
P FBR017 Fibrosarcoma 55 0.127
251
HYP014 Hyperuricemia 51 0.127
252
URT001 Urethritis 52 0.127
253
CHL068 Cholestasis 61 0.127
254
P MLN007 Male Infertility 56 0.127
255
P DRR001 Diarrhea 55 0.127
256
P ECL001 Eclampsia 52 0.127
257
P CNJ013 Conjunctivitis 66 0.127
258
CNN005 Connective Tissue Disease 66 0.127
259
P KDN018 Kidney Disease 71 0.127
260
P HPT021 Hepatitis 68 0.127
261
TRN015 Transient Cerebral Ischemia 62 0.127
262
P HYP086 Hypothyroidism 68 0.127
263
c HPT001 Hepatitis C 61 0.127
264
P PLY019 Polyneuropathy 52 0.127
265
SQM002 Squamous Cell Papilloma 45 0.127
266
P DMN001 Diamond-Blackfan Anemia 73 0.127
267
P GLM007 Glomerulonephritis 59 0.127
268
NWC001 Newcastle Disease 47 0.127
269
P KDN017 Kidney Cancer 60 0.127
270
CLC001 Calciphylaxis 50 0.127
271
P GST044 Gastritis 55 0.127
272
SKN020 Skin Papilloma 40 0.127
273
TRT001 Teratocarcinoma 41 0.127
274
EMB004 Embryonal Carcinoma 55 0.127
275
P SKN015 Skin Carcinoma 71 0.127
276
BNG036 Bone Giant Cell Tumor 48 0.127
277
GTR002 Goiter 52 0.127
278
P RNL015 Renal Hypertension 45 0.127
279
MCR018 Microcytic Anemia 46 0.127
280
CRT013 Carotid Stenosis 51 0.127
281
CHG001 Chagas Disease 65 0.127
282
CHL014 Cholera 62 0.127
283
ADL030 Adult-Onset Still's Disease 59 0.127
284
P CRD246 Cardiovascular System Disease 55 0.127
285
P FML340 Familial Episodic Pain Syndrome 50 0.127
286
P DRM010 Dermatomyositis 61 0.127
287
CRY005 Cryptococcosis 61 0.127
288
c SVR005 Severe Pre-Eclampsia 49 0.127
289
P MLN008 Melanoma 75 0.127
290
SCR011 Scrapie 39 0.127
291
P PRN023 Prion Disease 60 0.127
292
P LCT001 Lactic Acidosis 50 0.127
293
SNL007 Senile Cataract 40 0.127
294
CYT002 Cytokine Deficiency 43 0.127
295
FTT001 Fatty Liver Disease 61 0.127
296
STM007 Stomatitis 52 0.127
297
ORL006 Oral Mucosa Leukoplakia 22 0.127
298
CRH001 Crohn's Disease 80 0.127
299
c FML324 Familial Porphyria Cutanea Tarda 29 0.127
300
ALL014 Allergic Encephalomyelitis 34 0.127
301
P HYP076 Hyperthyroidism 53 0.127
302
CRT015 Carotid Artery Occlusion 45 0.127
303
ASB003 Asbestos Intoxication 32 0.127
304
CHR178 Chromosomal Triplication 33 0.127
305
CRT033 Corticobasal Degeneration 48 0.127
306
HVY002 Heavy Metal Poisoning 22 0.127
307
ARG004 Argyria 26 0.127
308
LKP003 Leukoplakia 39 0.127
309
P TRM003 Tremor 50 0.127
310
c RNG015 Ring Chromosome 2 22 0.127
311
P ENC018 Encephalopathy 62 0.127
Content
Loading form....