Search results for "hematuria"

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

259 hits were found for 'hematuria'

# Family MCID Name MIFTS Score
1
HMT008 Hematuria, Benign Familial 42 7.658
2
P ALP004 Alport Syndrome 69 4.706
3
LNP001 Loin Pain Hematuria Syndrome 11 3.580
4
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 28 3.248
5
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 26 3.248
6
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 2 2.343
7
CLB014 Coloboma, Cleft Lip/palate and Mental Retardation Syndrome 7 2.264
8
SCH014 Schistosomiasis 58 0.138
9
URN003 Urinary Schistosomiasis 48 0.113
10
P MMB011 Membranous Nephropathy 54 0.106
11
URN009 Urinary System Disease 50 0.098
12
P URF003 Urofacial Syndrome 1 50 0.098
13
P GLM007 Glomerulonephritis 59 0.089
14
P HMP007 Hemophilia 57 0.089
15
P CYS018 Cystitis 52 0.089
16
PYR004 Pyuria 32 0.089
17
P GLM015 Glomerulopathy with Fibronectin Deposits 2 22 0.089
18
ADN018 Adenoma 58 0.080
19
NLP001 Nail-Patella Syndrome 54 0.080
20
TRN018 Transitional Cell Carcinoma 53 0.080
21
GDP001 Goodpasture Syndrome 51 0.080
22
HYD002 Hydronephrosis 47 0.080
23
NPH001 Nephrogenic Adenoma 30 0.080
24
ESN013 Eosinophilic Cystitis 15 0.080
25
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.069
26
TBR010 Tuberculosis 70 0.069
27
P ADN016 Adenocarcinoma 69 0.069
28
ART016 Aortic Aneurysm 69 0.069
29
URN008 Urinary Bladder Cancer 66 0.069
30
CYS013 Cystinuria 63 0.069
31
FCT003 Factor X Deficiency 61 0.069
32
P DNT015 Dent Disease 61 0.069
33
P CTR002 Cataract 58 0.069
34
ANR040 Aneurysm 57 0.069
35
PRS047 Prostatitis 56 0.069
36
HMG005 Hemoglobinopathy 52 0.069
37
BLD044 Bladder Disease 51 0.069
38
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 0.069
39
c MLG069 Malignant Hypertension 47 0.069
40
INT067 Interstitial Nephritis 46 0.069
41
c ALP073 Alport Syndrome, Autosomal Recessive 43 0.069
42
c ALP074 Alport Syndrome, Autosomal Dominant 43 0.069
43
c ACQ014 Acquired Hemophilia 42 0.069
44
LMY003 Leiomyomatosis 42 0.069
45
CMP042 Complement Factor H Deficiency 41 0.069
46
URT001 Urethritis 41 0.069
47
RNL012 Renal Tuberculosis 40 0.069
48
c CNG029 Congenital Mesoblastic Nephroma 37 0.069
49
P CRY007 Cryoglobulinemia, Familial Mixed 35 0.069
50
c LPD019 Lipodystrophy, Partial, Acquired 33 0.069
51
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 21 0.069
52
MCP039 Mucoepithelial Dysplasia, Hereditary 17 0.069
53
NPH066 Nephropathy Due to Cfhr5 Deficiency 16 0.069
54
NPH008 Nephrogenic Adenoma of the Urethra 15 0.069
55
c SYS001 Systemic Lupus Erythematosus 86 0.056
56
P LKM002 Leukemia 71 0.056
57
FBR012 Fabry Disease 69 0.056
58
P TBR001 Tuberous Sclerosis 67 0.056
59
P LYM007 Lymphangioleiomyomatosis 66 0.056
60
P AMY004 Amyloidosis 65 0.056
61
P LPS004 Lupus Erythematosus 64 0.056
62
c HMP029 Hemophilia a 63 0.056
63
WLM007 Wilms Tumor Susceptibility-5 63 0.056
64
WGN006 Wegener Granulomatosis 63 0.056
65
CHR063 Chronic Mucocutaneous Candidiasis 63 0.056
66
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.056
67
P GCH001 Gaucher's Disease 62 0.056
68
LSC001 Lesch-Nyhan Syndrome 61 0.056
69
LWS003 Lowe Syndrome 61 0.056
70
P NPH009 Nephrolithiasis 60 0.056
71
P TMP003 Temporal Arteritis 60 0.056
72
P HMN010 Hemangioma 59 0.056
73
LGN002 Legionellosis 59 0.056
74
P NPH012 Nephrotic Syndrome 59 0.056
75
c GCH015 Gaucher Disease, Type I 59 0.056
76
PLS011 Plasmacytoma 56 0.056
77
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.056
78
NRM003 Norum Disease 51 0.056
79
P PTS002 Ptosis 51 0.056
80
HYP005 Hypokalemia 51 0.056
81
P PLY017 Polyarteritis Nodosa 51 0.056
82
RLP001 Relapsing Polychondritis 50 0.056
83
RHB001 Rhabdoid Cancer 50 0.056
84
MCR088 Microscopic Polyangiitis 49 0.056
85
HMG002 Hemoglobinuria 48 0.056
86
IGG001 Iga Glomerulonephritis 48 0.056
87
ANG018 Angiomyolipoma 46 0.056
88
c GCH017 Gaucher Disease, Type Iii 46 0.056
89
P ABD003 Abdominal Aortic Aneurysm 45 0.056
90
SPL018 Splenomegaly 44 0.056
91
VGN023 Vaginitis 42 0.056
92
MDL009 Medullary Sponge Kidney 41 0.056
93
MRB001 Marburg Hemorrhagic Fever 41 0.056
94
c ACQ042 Acquired Hemophilia a 40 0.056
95
ESN020 Eosinophilic Granulomatosis with Polyangiitis 39 0.056
96
RTR011 Retroperitoneal Fibrosis 39 0.056
97
RVL002 Ruvalcaba Syndrome 39 0.056
98
SML031 Small Cell Carcinoma of the Bladder 37 0.056
99
MJD001 Majeed Syndrome 33 0.056
100
HMR023 Hemorrhagic Cystitis 33 0.056
101
HYP193 Hypocomplementemic Urticarial Vasculitis 31 0.056
102
IMM073 Immunoglobulin a Vasculitis 29 0.056
103
MLK004 Malakoplakia 28 0.056
104
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 0.056
105
P IGN003 Iga Nephropathy 1 27 0.056
106
c GLM039 Glomerulosclerosis, Focal Segmental, 6 27 0.056
107
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 22 0.056
108
AND005 Androgen Insensitivity Syndrome, Mild 16 0.056
109
c GLM014 Glomerulopathy with Fibronectin Deposits 1 14 0.056
110
ANG062 Angioosteohypertrophic Syndrome 14 0.056
111
TRN046 Transverse Vaginal Septum 14 0.056
112
DYS180 Dyschondrosteosis and Nephritis 13 0.056
113
P CNG326 Congenital Primary Megaureter 12 0.056
114
CNG330 Congenital Megacalycosis 12 0.056
115
P RHM011 Rheumatoid Arthritis 89 0.040
116
P MLT019 Multiple Myeloma 83 0.040
117
P RNL014 Renal Cell Carcinoma 82 0.040
118
P ART022 Arthritis 75 0.040
119
WLS001 Wilson Disease 72 0.040
120
SCK003 Sickle Cell Anemia 71 0.040
121
P RSP003 Respiratory Failure 71 0.040
122
P NRB001 Neuroblastoma 70 0.040
123
P HPT021 Hepatitis 69 0.040
124
P KDN018 Kidney Disease 66 0.040
125
ART005 Arteriovenous Malformation 66 0.040
126
SRC014 Sarcoma 66 0.040
127
P THR014 Thrombocytopenia 64 0.040
128
P INF037 Inflammatory Bowel Disease 63 0.040
129
GLN010 Glanzmann Thrombasthenia 63 0.040
130
c HMP004 Hemophilia B 62 0.040
131
P HML002 Hemolytic Anemia 62 0.040
132
CNG368 Congenital Adrenal Hyperplasia 62 0.040
133
VNW001 Von Willebrand's Disease 61 0.040
134
FCT007 Factor Vii Deficiency 61 0.040
135
P SYS005 Systemic Scleroderma 61 0.040
136
P FCL005 Focal Segmental Glomerulosclerosis 60 0.040
137
P PRT013 Portal Hypertension 60 0.040
138
c ACT073 Acute Leukemia 60 0.040
139
GST045 Gastroenteritis 59 0.040
140
PRP030 Purpura 58 0.040
141
ADM013 Adamantinoma of Long Bones 57 0.040
142
P HMR003 Hemorrhagic Disease 57 0.040
143
SNS001 Sensorineural Hearing Loss 57 0.040
144
P SZR006 Seizure Disorder 56 0.040
145
P SML001 Small Cell Carcinoma 56 0.040
146
DSM004 Desmoid Tumor 56 0.040
147
CHR285 Chronic Myelomonocytic Leukemia 56 0.040
148
END030 End Stage Renal Failure 55 0.040
149
P TRM003 Tremor 54 0.040
150
P THY032 Thyroiditis 54 0.040
151
LYM022 Lymphangioma 54 0.040
152
P HYP620 Hypoprothrombinemia 54 0.040
153
P END033 Endocarditis 54 0.040
154
P PLY014 Polycystic Kidney Disease 53 0.040
155
P EXP004 Exophthalmos 53 0.040
156
P PYL005 Pyelonephritis 52 0.040
157
PRS042 Prostate Disease 52 0.040
158
PPL002 Papillary Carcinoma 51 0.040
159
BLD131 Bladder Urothelial Carcinoma 51 0.040
160
CLF001 Cleft Lip 50 0.040
161
RTN023 Retinitis 50 0.040
162
MCN001 Mucinous Adenocarcinoma 50 0.040
163
c ACT068 Acute Cystitis 50 0.040
164
NRG002 Neurogenic Bladder 50 0.040
165
P MTH008 Methylmalonic Acidemia 49 0.040
166
EXT010 Extramedullary Plasmacytoma 49 0.040
167
c ALM001 Al Amyloidosis 49 0.040
168
P FNC004 Fanconi Syndrome 49 0.040
169
ORT008 Orotic Aciduria 48 0.040
170
c HMG001 Hemoglobin C Disease 47 0.040
171
P HML033 Hemolytic Uremic Syndrome, Atypical 1 47 0.040
172
c PST041 Posterior Urethral Valves 47 0.040
173
GNG002 Ganglioneuroma 47 0.040
174
HMS001 Hemosiderosis 46 0.040
175
BLD053 Blood Platelet Disease 46 0.040
176
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 46 0.040
177
CLF004 Cleft Lip/palate 46 0.040
178
INT017 Intestinal Schistosomiasis 45 0.040
179
ANR004 Anuria 45 0.040
180
P AMY082 Amyloidosis, Familial Visceral 45 0.040
181
URT010 Ureteral Obstruction 45 0.040
182
VSC047 Vascular Malformation 45 0.040
183
TRC012 Trichuriasis 45 0.040
184
c ACT042 Acute Pyelonephritis 45 0.040
185
HNC001 Henoch-Schoenlein Purpura 45 0.040
186
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.040
187
P PLM085 Pulmonary Hemosiderosis 44 0.040
188
P ART084 Arteriovenous Fistula 44 0.040
189
FBR032 Fibromuscular Dysplasia 43 0.040
190
P PRL003 Proliferative Glomerulonephritis 43 0.040
191
CLN003 Clonorchiasis 43 0.040
192
MSN001 Mesangial Proliferative Glomerulonephritis 43 0.040
193
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 43 0.040
194
NPH010 Nephrosclerosis 43 0.040
195
DDN006 Duodenitis 42 0.040
196
TBL003 Tubular Adenocarcinoma 42 0.040
197
BLD130 Bladder Exstrophy 42 0.040
198
P BLD051 Blood Coagulation Disease 42 0.040
199
VGN020 Vaginal Disease 41 0.040
200
ANH002 Anhidrosis 41 0.040
201
CYS036 Cystinosis, Nephropathic 41 0.040
202
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.040
203
ASC002 Ascariasis 39 0.040
204
c HYP617 Hyperoxaluria, Primary, Type 1 39 0.040
205
THR035 Thrombasthenia 39 0.040
206
EPS006 Epstein Syndrome 39 0.040
207
HRM002 Hermaphroditism 38 0.040
208
SCR015 Scarlet Fever 38 0.040
209
DNS007 Dense Deposit Disease 37 0.040
210
FCH003 Fechtner Syndrome 37 0.040
211
ANG037 Angiomatosis 37 0.040
212
c SBC003 Subacute Bacterial Endocarditis 36 0.040
213
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 35 0.040
214
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.040
215
c CRN146 Corneal Dystrophy, Posterior Polymorphous, 3 35 0.040
216
PYL004 Pyelitis 35 0.040
217
CTN013 Cutaneous Anthrax 34 0.040
218
MLR007 Male Reproductive System Disease 34 0.040
219
HRS011 Horseshoe Kidney 33 0.040
220
P HYP111 Hyperprolinemia 33 0.040
221
PLV001 Pelvic Lipomatosis 33 0.040
222
c NPH046 Nephrolithiasis, Type I 32 0.040
223
ACT040 Acute Poststreptococcal Glomerulonephritis 32 0.040
224
URT020 Ureterocele 32 0.040
225
c HYP602 Hyperoxaluria, Primary, Type Ii 31 0.040
226
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 30 0.040
227
VSC008 Vascular Hemostatic Disease 30 0.040
228
C3G002 C3 Glomerulopathy 29 0.040
229
P HYP534 Hypomagnesemia 3, Renal 29 0.040
230
c GLM027 Glomerulosclerosis, Focal Segmental, 3 28 0.040
231
c HRD142 Hereditary Xanthinuria 28 0.040
232
c HML035 Hemolytic Uremic Syndrome, Atypical 2 27 0.040
233
c HML034 Hemolytic Uremic Syndrome, Atypical 3 27 0.040
234
c HML037 Hemolytic Uremic Syndrome, Atypical 5 26 0.040
235
c HML032 Hemolytic Uremic Syndrome, Atypical 4 26 0.040
236
c HYP603 Hyperoxaluria, Primary, Type Iii 25 0.040
237
c HML036 Hemolytic Uremic Syndrome, Atypical 6 25 0.040
238
HMX002 Heme Oxygenase-1 Deficiency 25 0.040
239
DFN256 Deafness and Myopia 25 0.040
240
P C1Q005 C1q Nephropathy 24 0.040
241
GLN006 Glandular Cystitis 23 0.040
242
IMM053 Immunotactoid Glomerulopathy 22 0.040
243
c GLY017 Glycogen Storage Disease Ic 21 0.040
244
INT258 Interstitial Nephritis, Karyomegalic 21 0.040
245
FBR085 Fibrillary Glomerulonephritis 20 0.040
246
URC005 Urachal Cyst 20 0.040
247
GNT004 Gnathomiasis 20 0.040
248
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 19 0.040
249
RNL089 Renal Nutcracker Syndrome 18 0.040
250
HGH021 Hughes-Stovin Syndrome 18 0.040
251
c RNL113 Renal Failure, Progressive, with Hypertension 18 0.040
252
URC004 Urachal Cancer 16 0.040
253
XLN198 X-Linked Diffuse Leiomyomatosis-Alport Syndrome 16 0.040
254
c IGN004 Iga Nephropathy 3 14 0.040
255
HYD031 Hydroxyprolinemia 12 0.040
256
INF059 Infundibulopelvic Dysgenesis 12 0.040
257
ANG064 Angioma, Hereditary Neurocutaneous Spinal Arterial Venous Malformations with Cutaneous Hemangiomas, Included 11 0.040
258
IMM051 Immunotactoid or Fibrillary Glomerulopathy 9 0.040
259
THR040 Thrombocytopenia with Elevated Serum Iga and Renal Disease 5 0.040