Search results for "hematuria"

The MalaCard for "hematuria" has been retired.
Searching MalaCards for entries containing "hematuria"

311 hits were found for 'hematuria'

# Family MCID Name MIFTS Score
1
HMT008 Hematuria, Benign Familial 35 7.245
2
P ALP004 Alport Syndrome 66 4.579
3
LNP001 Loin Pain Hematuria Syndrome 17 3.322
4
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 30 3.248
5
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 26 3.227
6
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 1 2.340
7
CLB014 Coloboma, Cleft Lip/palate and Mental Retardation Syndrome 8 2.265
8
P GLM015 Glomerulopathy with Fibronectin Deposits 2 24 0.084
9
P CYS013 Cystinuria 63 0.075
10
P THY032 Thyroiditis 49 0.075
11
GDP001 Goodpasture Syndrome 48 0.075
12
P OBS005 Obesity 87 0.065
13
P LKM002 Leukemia 63 0.065
14
CHR063 Chronic Mucocutaneous Candidiasis 59 0.065
15
NLP001 Nail-Patella Syndrome 58 0.065
16
FCT003 Factor X Deficiency 55 0.065
17
P TMP003 Temporal Arteritis 54 0.065
18
ADN024 Adenine Phosphoribosyltransferase Deficiency 48 0.065
19
CRB009 Cerebritis 44 0.065
20
END072 Endotheliitis 41 0.065
21
c ALP073 Alport Syndrome, Autosomal Recessive 41 0.065
22
c ALP074 Alport Syndrome, Autosomal Dominant 37 0.065
23
URN009 Urinary System Disease 35 0.065
24
CMP042 Complement Factor H Deficiency 31 0.065
25
c LPD019 Lipodystrophy, Partial, Acquired 31 0.065
26
MLK004 Malakoplakia 30 0.065
27
HRD052 Hereditary Mucoepithelial Dysplasia 24 0.065
28
NPH066 Nephropathy Due to Cfhr5 Deficiency 16 0.065
29
P BRS047 Breast Cancer 100 0.053
30
P LNG032 Lung Cancer 91 0.053
31
P PRS040 Prostate Cancer 87 0.053
32
c SYS001 Systemic Lupus Erythematosus 84 0.053
33
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.053
34
FBR012 Fabry Disease 67 0.053
35
P HPT021 Hepatitis 63 0.053
36
P PSD087 Pseudoxanthoma Elasticum 63 0.053
37
P LYM007 Lymphangioleiomyomatosis 63 0.053
38
LSC001 Lesch-Nyhan Syndrome 61 0.053
39
URN008 Urinary Bladder Cancer 60 0.053
40
WLM007 Wilms Tumor Susceptibility-5 58 0.053
41
WGN006 Wegener Granulomatosis 57 0.053
42
LGN002 Legionellosis 56 0.053
43
P GCH001 Gaucher's Disease 56 0.053
44
c EHL057 Ehlers-Danlos Syndrome, Type Iv 56 0.053
45
ATH003 Atherosclerosis 56 0.053
46
MLN008 Melanoma 55 0.053
47
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.053
48
LWS003 Lowe Syndrome 54 0.053
49
P ESP024 Esophagitis 54 0.053
50
PRS047 Prostatitis 53 0.053
51
ADN018 Adenoma 53 0.053
52
P GLM007 Glomerulonephritis 50 0.053
53
NRM003 Norum Disease 50 0.053
54
RLP001 Relapsing Polychondritis 49 0.053
55
BLD044 Bladder Disease 47 0.053
56
c GCH015 Gaucher Disease, Type I 47 0.053
57
ANR040 Aneurysm 46 0.053
58
RHB001 Rhabdoid Cancer 44 0.053
59
MCR088 Microscopic Polyangiitis 44 0.053
60
RTN023 Retinitis 42 0.053
61
PRS055 Pierson Syndrome 40 0.053
62
c GCH017 Gaucher Disease, Type Iii 39 0.053
63
MRB001 Marburg Hemorrhagic Fever 39 0.053
64
GRW007 Growth Hormone Deficiency 39 0.053
65
LMY003 Leiomyomatosis 39 0.053
66
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 37 0.053
67
ESN020 Eosinophilic Granulomatosis with Polyangiitis 35 0.053
68
MJD001 Majeed Syndrome 33 0.053
69
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 33 0.053
70
RVL002 Ruvalcaba Syndrome 32 0.053
71
HMR023 Hemorrhagic Cystitis 31 0.053
72
ACT100 Acute Febrile Neutrophilic Dermatosis 31 0.053
73
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 28 0.053
74
c GLM039 Glomerulosclerosis, Focal Segmental, 6 28 0.053
75
P IGN003 Iga Nephropathy 1 27 0.053
76
SML031 Small Cell Carcinoma of the Bladder 26 0.053
77
c NPH046 Nephrolithiasis, Type I 25 0.053
78
IMM073 Immunoglobulin a Vasculitis 23 0.053
79
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 19 0.053
80
c BNG076 Benign Exophthalmos Syndrome 17 0.053
81
AND005 Androgen Insensitivity Syndrome, Mild 17 0.053
82
ANG062 Angioosteohypertrophic Syndrome 15 0.053
83
NPH024 Nephrosis Deafness Urinary Tract Digital Malformation 15 0.053
84
c GLM014 Glomerulopathy with Fibronectin Deposits 1 15 0.053
85
P CNG326 Congenital Primary Megaureter 13 0.053
86
P CLR023 Colorectal Cancer 91 0.037
87
HPT023 Hepatocellular Carcinoma 87 0.037
88
P RNL014 Renal Cell Carcinoma 81 0.037
89
HV1006 Hiv-1 78 0.037
90
P AST005 Asthma 77 0.037
91
P MYC007 Myocardial Infarction 77 0.037
92
P RTN008 Retinitis Pigmentosa 75 0.037
93
P RTT002 Rett Syndrome 71 0.037
94
P PHC003 Pheochromocytoma 70 0.037
95
P APL001 Aplastic Anemia 68 0.037
96
P FML011 Familial Adenomatous Polyposis 67 0.037
97
ADN021 Adenomatous Polyposis Coli 67 0.037
98
INS024 Insulin-Like Growth Factor I 67 0.037
99
SCK003 Sickle Cell Anemia 66 0.037
100
P KRT004 Keratitis 66 0.037
101
P STM004 Stomach Cancer 66 0.037
102
ACH004 Achondroplasia 65 0.037
103
GLN010 Glanzmann Thrombasthenia 62 0.037
104
c SPN225 Spondyloarthropathy 1 61 0.037
105
P OST001 Osteopetrosis 61 0.037
106
P MYL006 Myeloid Leukemia 61 0.037
107
SRC014 Sarcoma 61 0.037
108
ART016 Aortic Aneurysm 60 0.037
109
P CRT072 Creutzfeldt-Jakob Disease 60 0.037
110
P LVR013 Liver Disease 60 0.037
111
AND015 Androgen Insensitivity 60 0.037
112
P HRP006 Herpes Simplex 59 0.037
113
ANX002 Anxiety Disorder 59 0.037
114
PRT036 Peritonitis 59 0.037
115
P AGM001 Agammaglobulinemia 59 0.037
116
P CRD011 Cardiomyopathy 59 0.037
117
P LPS004 Lupus Erythematosus 59 0.037
118
c BSL007 Basal Cell Carcinoma 59 0.037
119
c ATM003 Autoimmune Thyroiditis 59 0.037
120
P BPL003 Bipolar Disorder 59 0.037
121
P DYS007 Dyskeratosis Congenita 59 0.037
122
P ADN016 Adenocarcinoma 59 0.037
123
P PSR002 Psoriasis 58 0.037
124
ART005 Arteriovenous Malformation 57 0.037
125
P SYS005 Systemic Scleroderma 57 0.037
126
c HPT016 Hepatitis B 57 0.037
127
P AST007 Astrocytoma 57 0.037
128
CRB011 Cerebrotendinous Xanthomatosis 57 0.037
129
SCH014 Schistosomiasis 57 0.037
130
TKY001 Takayasu's Arteritis 56 0.037
131
P PNM007 Pneumonia 56 0.037
132
P NPH012 Nephrotic Syndrome 55 0.037
133
P MNN013 Meningitis 55 0.037
134
P HYP061 Hypertrophic Cardiomyopathy 55 0.037
135
P PRM002 Primary Hyperoxaluria 55 0.037
136
P CND004 Candidiasis 55 0.037
137
HRP004 Herpes Zoster 55 0.037
138
P OST009 Osteochondritis Dissecans 54 0.037
139
P MSC005 Muscular Dystrophy 54 0.037
140
DNY001 Denys-Drash Syndrome 54 0.037
141
P MYP004 Myopathy 54 0.037
142
P INF032 Infertility 54 0.037
143
APH001 Aphthous Stomatitis 53 0.037
144
P DNT015 Dent Disease 53 0.037
145
P CRN012 Craniometaphyseal Dysplasia 53 0.037
146
VSC011 Vasculitis 53 0.037
147
CYS010 Cystinosis 53 0.037
148
P MTH008 Methylmalonic Acidemia 52 0.037
149
P THR003 Thoracic Aortic Aneurysm 52 0.037
150
P CNJ013 Conjunctivitis 52 0.037
151
PTY003 Pityriasis Rubra Pilaris 52 0.037
152
P HYP620 Hypoprothrombinemia 52 0.037
153
c SVR001 Severe Acute Respiratory Syndrome 52 0.037
154
P ESN007 Eosinophilia 52 0.037
155
P FBR017 Fibrosarcoma 51 0.037
156
ORT008 Orotic Aciduria 51 0.037
157
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.037
158
WLF002 Wolf-Hirschhorn Syndrome 51 0.037
159
FDL002 Food Allergy 51 0.037
160
DMN002 Dementia 51 0.037
161
THY103 Thyroid Cancer, Monmedullary, 1 50 0.037
162
GST040 Gastric Adenocarcinoma 50 0.037
163
P PRM006 Primary Biliary Cirrhosis 50 0.037
164
TRN018 Transitional Cell Carcinoma 50 0.037
165
END030 End Stage Renal Failure 50 0.037
166
MGL001 Megaloblastic Anemia 49 0.037
167
CLT003 Colitis 49 0.037
168
GTR002 Goiter 49 0.037
169
ART111 Artery Disease 49 0.037
170
NSP002 Nasopharyngitis 48 0.037
171
ALL009 Allergic Conjunctivitis 48 0.037
172
CHC001 Chickenpox 48 0.037
173
P NPH009 Nephrolithiasis 48 0.037
174
MLN007 Male Infertility 47 0.037
175
PLM014 Pleomorphic Adenoma 47 0.037
176
P HYP065 Hyperaldosteronism 47 0.037
177
P CTR002 Cataract 47 0.037
178
P NRP001 Neuropathy 47 0.037
179
ANN002 Anencephaly 46 0.037
180
HNT002 Hantavirus Pulmonary Syndrome 46 0.037
181
GST045 Gastroenteritis 46 0.037
182
HYP266 Hypoxia 46 0.037
183
PYD001 Pyoderma Gangrenosum 45 0.037
184
DYS014 Dyspepsia 45 0.037
185
STM007 Stomatitis 45 0.037
186
CHN016 Cohen Syndrome 45 0.037
187
SPN020 Spondylosis 45 0.037
188
P RNV001 Renovascular Hypertension 44 0.037
189
LYM027 Lymphopenia 44 0.037
190
P PNC001 Pancytopenia 44 0.037
191
CRB016 Carbuncle 43 0.037
192
PYR010 Peyronie's Disease 43 0.037
193
SLP001 Sleeping Sickness 43 0.037
194
FCL012 Facial Paralysis 43 0.037
195
P END046 Endometritis 43 0.037
196
ANK001 Ankylosis 42 0.037
197
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 42 0.037
198
ANR004 Anuria 42 0.037
199
FBR032 Fibromuscular Dysplasia 42 0.037
200
P PLY041 Polymyositis 42 0.037
201
P INT030 Intracranial Aneurysm 41 0.037
202
P MMB011 Membranous Nephropathy 41 0.037
203
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 41 0.037
204
RNL078 Renal Dysplasia 41 0.037
205
c ACT134 Acute Liver Failure 41 0.037
206
RNL077 Renal Fibrosis 40 0.037
207
P AMY082 Amyloidosis, Familial Visceral 40 0.037
208
P GND004 Gonadal Dysgenesis 40 0.037
209
c ACT068 Acute Cystitis 40 0.037
210
PRP080 Peripheral Artery Disease 40 0.037
211
PNM008 Pneumothorax 40 0.037
212
PYD002 Pyoderma 40 0.037
213
FCT005 Factor Xiii Deficiency 40 0.037
214
PRS042 Prostate Disease 40 0.037
215
CHL004 Cholelithiasis 39 0.037
216
XNT003 Xanthomatosis 39 0.037
217
CRS001 Crescentic Glomerulonephritis 39 0.037
218
PLY020 Polyradiculoneuropathy 39 0.037
219
FCH003 Fechtner Syndrome 39 0.037
220
CHR177 Chromophobe Renal Cell Carcinoma 38 0.037
221
FRN002 Frontal Lobe Epilepsy 38 0.037
222
GRN039 Greenberg Skeletal Dysplasia 38 0.037
223
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 38 0.037
224
c RTN058 Retinitis Pigmentosa 3 37 0.037
225
INT025 Intermittent Explosive Disorder 37 0.037
226
c HYP617 Hyperoxaluria, Primary, Type 1 37 0.037
227
P BLD051 Blood Coagulation Disease 37 0.037
228
ORN001 Ornithosis 36 0.037
229
P CYS036 Cystinosis, Nephropathic 36 0.037
230
ADR041 Adrenal Cortical Adenoma 36 0.037
231
NRN002 Neuronitis 36 0.037
232
P ARC016 Auriculocondylar Syndrome 1 35 0.037
233
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 35 0.037
234
EPS006 Epstein Syndrome 35 0.037
235
CRY021 Cryoglobulinemic Vasculitis 35 0.037
236
DNS007 Dense Deposit Disease 35 0.037
237
c ACQ014 Acquired Hemophilia 35 0.037
238
BRS090 Breast Reconstruction 35 0.037
239
P STR021 Struma Ovarii 34 0.037
240
SPR012 Separation Anxiety Disorder 34 0.037
241
PLP001 Pulpitis 34 0.037
242
STR072 Stromal Keratitis 34 0.037
243
HYD005 Hydrocele 33 0.037
244
c ACQ042 Acquired Hemophilia a 33 0.037
245
WLL004 Wallerian Degeneration 33 0.037
246
c GLL024 Gallbladder Disease 1 33 0.037
247
NNT010 Nontoxic Goiter 32 0.037
248
PRS029 Periosteal Osteogenic Sarcoma 32 0.037
249
LNS001 Lens Subluxation 32 0.037
250
SKL007 Skeletal Muscle Regeneration 32 0.037
251
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 31 0.037
252
CRB004 Cerebral Artery Occlusion 31 0.037
253
c HML032 Hemolytic Uremic Syndrome, Atypical 4 31 0.037
254
P SLP003 Salpingitis 30 0.037
255
P CRN035 Cranial Nerve Palsy 30 0.037
256
PLV001 Pelvic Lipomatosis 29 0.037
257
EYL005 Eyelid Disease 29 0.037
258
AYM001 Ayme-Gripp Syndrome 29 0.037
259
c MLT009 Multiple Cranial Nerve Palsy 29 0.037
260
NRD001 Neurodermatitis 29 0.037
261
BSM001 Basement Membrane Disease 29 0.037
262
CNC001 Cancerophobia 29 0.037
263
c HRD142 Hereditary Xanthinuria 29 0.037
264
PRS037 Periostitis 28 0.037
265
LTM002 Luteoma 28 0.037
266
c HYP602 Hyperoxaluria, Primary, Type Ii 28 0.037
267
PYR004 Pyuria 28 0.037
268
ISC001 Ischemic Neuropathy 27 0.037
269
HMX002 Heme Oxygenase-1 Deficiency 27 0.037
270
FCT013 Factor V Leiden Thrombophilia 26 0.037
271
c HYP603 Hyperoxaluria, Primary, Type Iii 26 0.037
272
NCR009 Necrobiotic Xanthogranuloma 25 0.037
273
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 24 0.037
274
P HYP534 Hypomagnesemia 3, Renal 24 0.037
275
MLR007 Male Reproductive System Disease 24 0.037
276
SPN156 Spontaneous Coronary Artery Dissection 24 0.037
277
P SPR036 Supernumerary Nipples 24 0.037
278
GNT004 Gnathomiasis 24 0.037
279
c HML034 Hemolytic Uremic Syndrome, Atypical 3 23 0.037
280
C3G002 C3 Glomerulopathy 23 0.037
281
HRP011 Herpes Zoster Ophthalmicus 23 0.037
282
URC005 Urachal Cyst 23 0.037
283
INT258 Interstitial Nephritis, Karyomegalic 23 0.037
284
c HML036 Hemolytic Uremic Syndrome, Atypical 6 23 0.037
285
c HML037 Hemolytic Uremic Syndrome, Atypical 5 23 0.037
286
c GLM027 Glomerulosclerosis, Focal Segmental, 3 23 0.037
287
c HML035 Hemolytic Uremic Syndrome, Atypical 2 23 0.037
288
MLG085 Male Genital Disorders 22 0.037
289
MLL004 Mallory-Weiss Syndrome 22 0.037
290
IMM053 Immunotactoid Glomerulopathy 22 0.037
291
SLP002 Salpingitis Isthmica Nodosa 21 0.037
292
VSC008 Vascular Hemostatic Disease 21 0.037
293
DFN256 Deafness and Myopia 20 0.037
294
FBR085 Fibrillary Glomerulonephritis 20 0.037
295
c GLY017 Glycogen Storage Disease Ic 20 0.037
296
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 20 0.037
297
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 19 0.037
298
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 17 0.037
299
HYD031 Hydroxyprolinemia 17 0.037
300
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 17 0.037
301
RNL089 Renal Nutcracker Syndrome 16 0.037
302
HYP666 Hypoparathyroidism-Deafness-Renal Disease Syndrome 16 0.037
303
FML277 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis with Severe Ocular Involvement 15 0.037
304
SPR064 Supernumerary Breasts 14 0.037
305
URC004 Urachal Cancer 14 0.037
306
DYS034 Dyschondrosteosis Nephritis 10 0.037
307
SLC010 Salcedo Syndrome 10 0.037
308
UVL008 Uveal Coloboma-Cleft Lip and Palate-Intellectual Disability 10 0.037
309
IMM051 Immunotactoid or Fibrillary Glomerulopathy 9 0.037
310
INF059 Infundibulopelvic Dysgenesis 6 0.037
311
THR040 Thrombocytopenia with Elevated Serum Iga and Renal Disease 5 0.037