Search results for hematuria

306 hits were found for hematuria

# Family MCID Name MIFTS Score
1
HMT008 Hematuria, Benign Familial 40 8.617
2
ALP046 Alport Syndrome, X-Linked 74 4.713
3
LNP001 Loin Pain Hematuria Syndrome 14 3.551
4
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 30 3.301
5
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 2 2.334
6
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 24 2.314
7
UVL008 Uveal Coloboma-Cleft Lip and Palate-Intellectual Disability 18 2.314
8
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.218
9
SCH014 Schistosomiasis 62 0.130
10
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.124
11
URN009 Urinary System Disease 58 0.118
12
P MMB011 Membranous Nephropathy 55 0.106
13
URN003 Urinary Schistosomiasis 50 0.106
14
P GLM015 Glomerulopathy with Fibronectin Deposits 2 30 0.106
15
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.099
16
P BLD134 Bladder Cancer 78 0.092
17
P HMP007 Hemophilia 61 0.092
18
P GLM007 Glomerulonephritis 61 0.092
19
P CYS018 Cystitis 57 0.092
20
c ACQ014 Acquired Hemophilia 51 0.092
21
GDP001 Goodpasture Syndrome 55 0.084
22
P ALP074 Alport Syndrome, Autosomal Dominant 47 0.084
23
P IGN003 Iga Nephropathy 1 34 0.084
24
PYR004 Pyuria 34 0.084
25
MCP039 Mucoepithelial Dysplasia, Hereditary 30 0.084
26
CFH006 Cfhr5 Deficiency 16 0.084
27
P MYC084 Mycobacterium Tuberculosis 1 69 0.075
28
ADN018 Adenoma 63 0.075
29
TRN018 Transitional Cell Carcinoma 58 0.075
30
NLP001 Nail-Patella Syndrome 56 0.075
31
P DNT020 Dent Disease 1 55 0.075
32
c ALP073 Alport Syndrome, Autosomal Recessive 50 0.075
33
HYD002 Hydronephrosis 49 0.075
34
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.075
35
c HYP794 Hyperoxaluria, Primary, Type I 41 0.075
36
RNL012 Renal Tuberculosis 35 0.075
37
NPH001 Nephrogenic Adenoma 31 0.075
38
ESN013 Eosinophilic Cystitis 18 0.075
39
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.065
40
P ADN016 Adenocarcinoma 71 0.065
41
ART016 Aortic Aneurysm 70 0.065
42
c WLM013 Wilms Tumor 1 69 0.065
43
c HMP004 Hemophilia B 67 0.065
44
CYS013 Cystinuria 64 0.065
45
ANR040 Aneurysm 61 0.065
46
P CTR002 Cataract 60 0.065
47
PRS047 Prostatitis 59 0.065
48
FCT003 Factor X Deficiency 58 0.065
49
BLD044 Bladder Disease 55 0.065
50
HMG005 Hemoglobinopathy 53 0.065
51
INT067 Interstitial Nephritis 51 0.065
52
ANG018 Angiomyolipoma 50 0.065
53
ADN024 Adenine Phosphoribosyltransferase Deficiency 49 0.065
54
c MLG069 Malignant Hypertension 49 0.065
55
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 49 0.065
56
AMY082 Amyloidosis, Familial Visceral 47 0.065
57
LMY003 Leiomyomatosis 45 0.065
58
URT001 Urethritis 44 0.065
59
c CNG029 Congenital Mesoblastic Nephroma 43 0.065
60
CMP042 Complement Factor H Deficiency 39 0.065
61
c LPD019 Lipodystrophy, Partial, Acquired 38 0.065
62
c HYP534 Hypomagnesemia 3, Renal 37 0.065
63
HMR023 Hemorrhagic Cystitis 36 0.065
64
c HYP603 Hyperoxaluria, Primary, Type Iii 30 0.065
65
LMY010 Leiomyomatosis, Diffuse, with Alport Syndrome 23 0.065
66
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 22 0.065
67
c FCL043 Focal Segmental Glomerulosclerosis 6 21 0.065
68
c GLM014 Glomerulopathy with Fibronectin Deposits 1 18 0.065
69
c IGN004 Iga Nephropathy 3 17 0.065
70
c IGN002 Iga Nephropathy 2 17 0.065
71
NPH008 Nephrogenic Adenoma of the Urethra 15 0.065
72
c SYS001 Systemic Lupus Erythematosus 86 0.053
73
P LKM002 Leukemia 75 0.053
74
FBR012 Fabry Disease 72 0.053
75
WGN006 Wegener Granulomatosis 71 0.053
76
P LPS004 Lupus Erythematosus 69 0.053
77
P TBR001 Tuberous Sclerosis 69 0.053
78
P AMY004 Amyloidosis 69 0.053
79
c HMP029 Hemophilia a 69 0.053
80
P ANR048 Aniridia 1 68 0.053
81
LYM007 Lymphangioleiomyomatosis 68 0.053
82
P TMP003 Temporal Arteritis 67 0.053
83
CHR063 Chronic Mucocutaneous Candidiasis 66 0.053
84
LGN002 Legionellosis 65 0.053
85
c CHR417 Chronic Graft Versus Host Disease 65 0.053
86
AGN016 Aging 65 0.053
87
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.053
88
LWC002 Lowe Oculocerebrorenal Syndrome 62 0.053
89
P GCH001 Gaucher's Disease 62 0.053
90
LSC001 Lesch-Nyhan Syndrome 62 0.053
91
P HMN010 Hemangioma 61 0.053
92
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 0.053
93
P NPH012 Nephrotic Syndrome 60 0.053
94
PLS011 Plasmacytoma 60 0.053
95
P FCL005 Focal Segmental Glomerulosclerosis 60 0.053
96
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.053
97
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.053
98
VGN023 Vaginitis 59 0.053
99
MCR088 Microscopic Polyangiitis 58 0.053
100
c GCH015 Gaucher Disease, Type I 57 0.053
101
NPH009 Nephrolithiasis 57 0.053
102
RLP001 Relapsing Polychondritis 55 0.053
103
HYP005 Hypokalemia 53 0.053
104
c PNS012 Paine Syndrome 52 0.053
105
IGG001 Iga Glomerulonephritis 52 0.053
106
HMG002 Hemoglobinuria 52 0.053
107
P PLY017 Polyarteritis Nodosa 51 0.053
108
EPD077 Epidermolysis Bullosa Junctionalis with Pyloric Atresia 51 0.053
109
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 51 0.053
110
RHB001 Rhabdoid Cancer 51 0.053
111
ORT008 Orotic Aciduria 50 0.053
112
P PTS002 Ptosis 50 0.053
113
P HML033 Hemolytic Uremic Syndrome, Atypical 1 49 0.053
114
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.053
115
c GCH017 Gaucher Disease, Type Iii 47 0.053
116
CYS036 Cystinosis, Nephropathic 47 0.053
117
MDL009 Medullary Sponge Kidney 46 0.053
118
SPL018 Splenomegaly 45 0.053
119
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.053
120
c ACQ042 Acquired Hemophilia a 44 0.053
121
MRB001 Marburg Hemorrhagic Fever 43 0.053
122
RTR011 Retroperitoneal Fibrosis 43 0.053
123
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.053
124
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 40 0.053
125
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.053
126
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.053
127
FCH003 Fechtner Syndrome 38 0.053
128
HYP193 Hypocomplementemic Urticarial Vasculitis 38 0.053
129
RVL002 Ruvalcaba Syndrome 37 0.053
130
c HYP602 Hyperoxaluria, Primary, Type Ii 37 0.053
131
MJD001 Majeed Syndrome 35 0.053
132
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 34 0.053
133
MLK004 Malakoplakia 34 0.053
134
SML031 Small Cell Carcinoma of the Bladder 34 0.053
135
EPS006 Epstein Syndrome 33 0.053
136
BLD045 Bladder Diverticulum 32 0.053
137
DRG013 Drug-Induced Lupus Erythematosus 29 0.053
138
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 29 0.053
139
IMM073 Immunoglobulin a Vasculitis 28 0.053
140
INT258 Interstitial Nephritis, Karyomegalic 28 0.053
141
c GLY017 Glycogen Storage Disease Ic 28 0.053
142
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 0.053
143
c ALG016 Alagille Syndrome 2 26 0.053
144
ANG062 Angioosteohypertrophic Syndrome 25 0.053
145
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.053
146
c HML034 Hemolytic Uremic Syndrome, Atypical 3 22 0.053
147
c HML037 Hemolytic Uremic Syndrome, Atypical 5 22 0.053
148
c HML032 Hemolytic Uremic Syndrome, Atypical 4 22 0.053
149
c HML036 Hemolytic Uremic Syndrome, Atypical 6 22 0.053
150
c HML035 Hemolytic Uremic Syndrome, Atypical 2 22 0.053
151
ANR038 Anorexia Nervosa 1 21 0.053
152
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 21 0.053
153
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.053
154
PRT121 Proteinuria, Low Molecular Weight, with Hypercalciuria and Nephrocalcinosis 19 0.053
155
c NPH096 Nephrotic Syndrome, Type 12 19 0.053
156
DYS180 Dyschondrosteosis and Nephritis 18 0.053
157
HYD031 Hydroxyprolinemia 18 0.053
158
BLD137 Blood Group--Ahonen 17 0.053
159
ANG067 Angioma, Hereditary Neurocutaneous 17 0.053
160
c PTR011 Paternal Uniparental Disomy of Chromosome 1 16 0.053
161
NLP003 Nail-Patella-Like Renal Disease 16 0.053
162
CNG330 Congenital Megacalycosis 16 0.053
163
TRN046 Transverse Vaginal Septum 15 0.053
164
INF059 Infundibulopelvic Dysgenesis 15 0.053
165
P CNG326 Congenital Primary Megaureter 14 0.053
166
LPD043 Lipodystrophy, Partial, Acquired, with Low Complement Component C3, with or Without Glomerulonephritis 13 0.053
167
THR040 Thrombocytopenia with Elevated Serum Iga and Renal Disease 11 0.053
168
c CRY033 Cryofibrinogenemia, Familial Primary 10 0.053
169
P RHM011 Rheumatoid Arthritis 91 0.037
170
MYL069 Myeloma, Multiple 86 0.037
171
P HRT032 Heart Disease 80 0.037
172
P ART022 Arthritis 77 0.037
173
P HPT021 Hepatitis 75 0.037
174
SCK003 Sickle Cell Anemia 73 0.037
175
P NRB001 Neuroblastoma 73 0.037
176
VNH007 Von Hippel-Lindau Syndrome 72 0.037
177
P PHC003 Pheochromocytoma 72 0.037
178
P DBT009 Diabetes Mellitus 72 0.037
179
WLS001 Wilson Disease 72 0.037
180
P RSP003 Respiratory Failure 71 0.037
181
c JVN010 Juvenile Rheumatoid Arthritis 71 0.037
182
P KDN018 Kidney Disease 69 0.037
183
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.037
184
SRC014 Sarcoma 68 0.037
185
P SYS005 Systemic Scleroderma 67 0.037
186
P PRT008 Proteus Syndrome 67 0.037
187
P MCR115 Microvascular Complications of Diabetes 5 66 0.037
188
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.037
189
GLN010 Glanzmann Thrombasthenia 66 0.037
190
GST045 Gastroenteritis 65 0.037
191
P THR014 Thrombocytopenia 65 0.037
192
ART005 Arteriovenous Malformation 64 0.037
193
DSM004 Desmoid Tumor 63 0.037
194
P CHR285 Chronic Myelomonocytic Leukemia 63 0.037
195
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.037
196
P HML002 Hemolytic Anemia 62 0.037
197
FCT007 Factor Vii Deficiency 62 0.037
198
PRP030 Purpura 61 0.037
199
VNW001 Von Willebrand's Disease 61 0.037
200
P HMR003 Hemorrhagic Disease 61 0.037
201
c ACT073 Acute Leukemia 61 0.037
202
P PLY014 Polycystic Kidney Disease 60 0.037
203
P PRT013 Portal Hypertension 59 0.037
204
SNS001 Sensorineural Hearing Loss 59 0.037
205
END030 End Stage Renal Failure 59 0.037
206
P SML001 Small Cell Carcinoma 58 0.037
207
P END033 Endocarditis 58 0.037
208
c ALM001 Al Amyloidosis 56 0.037
209
P PYL005 Pyelonephritis 56 0.037
210
P ALP008 Alopecia 56 0.037
211
P THY032 Thyroiditis 56 0.037
212
MTH078 Methylmalonic Aciduria, Cblb Type 56 0.037
213
BLD131 Bladder Urothelial Carcinoma 55 0.037
214
P SZR006 Seizure Disorder 55 0.037
215
P FNC004 Fanconi Syndrome 54 0.037
216
CLF001 Cleft Lip 54 0.037
217
P TRM003 Tremor 54 0.037
218
MCN001 Mucinous Adenocarcinoma 54 0.037
219
NRG002 Neurogenic Bladder 53 0.037
220
LYM022 Lymphangioma 53 0.037
221
FBR032 Fibromuscular Dysplasia 53 0.037
222
EXT010 Extramedullary Plasmacytoma 52 0.037
223
P INF037 Inflammatory Bowel Disease 52 0.037
224
RTN023 Retinitis 52 0.037
225
HPT082 Hepatic Adenomas, Familial 52 0.037
226
CLB010 Coloboma of Macula 52 0.037
227
FCT006 Factor V Deficiency 52 0.037
228
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.037
229
PRT129 Prothrombin Deficiency, Congenital 51 0.037
230
PPL002 Papillary Carcinoma 51 0.037
231
c PST041 Posterior Urethral Valves 51 0.037
232
EXP004 Exophthalmos 50 0.037
233
GNG002 Ganglioneuroma 50 0.037
234
FCT001 Factor Viii Deficiency 50 0.037
235
HMS001 Hemosiderosis 50 0.037
236
TRC012 Trichuriasis 50 0.037
237
CLF004 Cleft Lip/palate 49 0.037
238
ANR004 Anuria 49 0.037
239
URT010 Ureteral Obstruction 49 0.037
240
P PLM085 Pulmonary Hemosiderosis 48 0.037
241
HNC001 Henoch-Schoenlein Purpura 48 0.037
242
c ACT042 Acute Pyelonephritis 48 0.037
243
INT017 Intestinal Schistosomiasis 47 0.037
244
PRS129 Prostatic Hyperplasia, Benign 47 0.037
245
P ART084 Arteriovenous Fistula 46 0.037
246
NPH010 Nephrosclerosis 46 0.037
247
CLN003 Clonorchiasis 46 0.037
248
DDN006 Duodenitis 46 0.037
249
THR035 Thrombasthenia 46 0.037
250
ANH002 Anhidrosis 45 0.037
251
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 45 0.037
252
EXS017 Exstrophy of Bladder 45 0.037
253
P PRL003 Proliferative Glomerulonephritis 45 0.037
254
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 44 0.037
255
c XNT010 Xanthinuria, Type I 43 0.037
256
TBL003 Tubular Adenocarcinoma 43 0.037
257
HRM002 Hermaphroditism 42 0.037
258
EST003 Eastern Equine Encephalitis 41 0.037
259
SCR015 Scarlet Fever 40 0.037
260
c CRN146 Corneal Dystrophy, Posterior Polymorphous, 3 40 0.037
261
P HYP761 Hypouricemia, Renal, 1 40 0.037
262
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.037
263
c HMG001 Hemoglobin C Disease 39 0.037
264
AND014 Androgenic Alopecia 39 0.037
265
P BLD051 Blood Coagulation Disease 38 0.037
266
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.037
267
PYL004 Pyelitis 38 0.037
268
c SBC003 Subacute Bacterial Endocarditis 38 0.037
269
ACT040 Acute Poststreptococcal Glomerulonephritis 37 0.037
270
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.037
271
P HYP733 Hypercalciuria, Absorptive, 2 37 0.037
272
URT020 Ureterocele 37 0.037
273
DNS007 Dense Deposit Disease 36 0.037
274
ANG037 Angiomatosis 36 0.037
275
P HYP111 Hyperprolinemia 36 0.037
276
PLV001 Pelvic Lipomatosis 35 0.037
277
HRS011 Horseshoe Kidney 35 0.037
278
CTN013 Cutaneous Anthrax 35 0.037
279
C3G002 C3 Glomerulopathy 34 0.037
280
c NPH031 Nephronophthisis 3 32 0.037
281
ALR002 Al-Raqad Syndrome 30 0.037
282
c HRD142 Hereditary Xanthinuria 30 0.037
283
URN022 Urinary Tract Infections, Recurrent 29 0.037
284
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.037
285
c RNL113 Renal Failure, Progressive, with Hypertension 29 0.037
286
FBR089 Fibrosclerosis, Multifocal 28 0.037
287
HMX003 Heme Oxygenase 1 Deficiency 26 0.037
288
GNT004 Gnathomiasis 26 0.037
289
DFN256 Deafness and Myopia 25 0.037
290
MYH015 Myh-9 Related Disease 24 0.037
291
RTN179 Retinal Arteries, Tortuosity of 23 0.037
292
IMM053 Immunotactoid Glomerulopathy 23 0.037
293
HGH021 Hughes-Stovin Syndrome 23 0.037
294
P C1Q005 C1q Nephropathy 23 0.037
295
FBR085 Fibrillary Glomerulonephritis 23 0.037
296
URC005 Urachal Cyst 22 0.037
297
c FCL027 Focal Segmental Glomerulosclerosis 3 20 0.037
298
RNL089 Renal Nutcracker Syndrome 20 0.037
299
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 18 0.037
300
GLN006 Glandular Cystitis 18 0.037
301
URC004 Urachal Cancer 18 0.037
302
NNF008 Non-Functioning Paraganglioma 17 0.037
303
CNG491 Congenital Portosystemic Shunt 15 0.037
304
IMM051 Immunotactoid or Fibrillary Glomerulopathy 12 0.037
305
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 11 0.037
306
c NPH101 Nephrotic Syndrome 16 11 0.037
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