Search results for "hematuria"

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

285 hits were found for 'hematuria'

# Family MCID Name MIFTS Score
1
HMT008 Hematuria, Benign Familial 32 6.887
2
P ALP004 Alport Syndrome 66 4.688
3
LNP001 Loin Pain Hematuria Syndrome 12 3.554
4
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 33 3.251
5
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 22 3.251
6
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 1 2.344
7
CLB014 Coloboma, Cleft Lip/palate and Mental Retardation Syndrome 7 2.267
8
SCH014 Schistosomiasis 55 0.134
9
URN003 Urinary Schistosomiasis 43 0.109
10
P MMB011 Membranous Nephropathy 43 0.102
11
P GLM007 Glomerulonephritis 49 0.095
12
BSM001 Basement Membrane Disease 26 0.095
13
PYR004 Pyuria 29 0.087
14
P GLM015 Glomerulopathy with Fibronectin Deposits 2 23 0.087
15
ADN018 Adenoma 54 0.077
16
GDP001 Goodpasture Syndrome 47 0.077
17
P CYS018 Cystitis 47 0.077
18
TRN018 Transitional Cell Carcinoma 44 0.077
19
URN009 Urinary System Disease 33 0.077
20
NPH001 Nephrogenic Adenoma 31 0.077
21
c SYS001 Systemic Lupus Erythematosus 90 0.067
22
P HRD008 Hereditary Hemorrhagic Telangiectasia 74 0.067
23
P CYS013 Cystinuria 67 0.067
24
c SPN225 Spondyloarthropathy 1 66 0.067
25
TBR010 Tuberculosis 64 0.067
26
NLP001 Nail-Patella Syndrome 59 0.067
27
FCT003 Factor X Deficiency 58 0.067
28
P KDN018 Kidney Disease 57 0.067
29
P ADN016 Adenocarcinoma 56 0.067
30
ART016 Aortic Aneurysm 55 0.067
31
P RHB017 Rhabdoid Tumor 54 0.067
32
P HMP007 Hemophilia 51 0.067
33
P CTR002 Cataract 48 0.067
34
c MLG069 Malignant Hypertension 46 0.067
35
ANR040 Aneurysm 43 0.067
36
ADN024 Adenine Phosphoribosyltransferase Deficiency 43 0.067
37
P HYD002 Hydronephrosis 42 0.067
38
INT067 Interstitial Nephritis 41 0.067
39
HMG005 Hemoglobinopathy 40 0.067
40
URT001 Urethritis 40 0.067
41
c ALP073 Alport Syndrome, Autosomal Recessive 40 0.067
42
CMP042 Complement Factor H Deficiency 37 0.067
43
c ALP074 Alport Syndrome, Autosomal Dominant 36 0.067
44
LMY003 Leiomyomatosis 36 0.067
45
RNL012 Renal Tuberculosis 36 0.067
46
c LPD019 Lipodystrophy, Partial, Acquired 34 0.067
47
HRD052 Hereditary Mucoepithelial Dysplasia 33 0.067
48
NPH008 Nephrogenic Adenoma of the Urethra 17 0.067
49
ESN013 Eosinophilic Cystitis 16 0.067
50
NPH066 Nephropathy Due to Cfhr5 Deficiency 14 0.067
51
FBR012 Fabry Disease 75 0.055
52
ANR002 Aniridia 72 0.055
53
P ANG001 Angelman Syndrome 66 0.055
54
P TBR001 Tuberous Sclerosis 65 0.055
55
LSC001 Lesch-Nyhan Syndrome 64 0.055
56
P GCH001 Gaucher's Disease 64 0.055
57
WLM007 Wilms Tumor Susceptibility-5 61 0.055
58
P LKM002 Leukemia 61 0.055
59
P LPS004 Lupus Erythematosus 61 0.055
60
P LYM007 Lymphangioleiomyomatosis 61 0.055
61
P AMY004 Amyloidosis 60 0.055
62
WGN006 Wegener Granulomatosis 59 0.055
63
c EHL057 Ehlers-Danlos Syndrome, Type Iv 58 0.055
64
BLD087 Bladder Cancer, Somatic 58 0.055
65
c GCH015 Gaucher Disease, Type I 56 0.055
66
ACN002 Acanthosis Nigricans 53 0.055
67
KLP010 Klippel-Trenaunay-Weber Syndrome 53 0.055
68
CHR001 Churg-Strauss Syndrome 53 0.055
69
P TMP003 Temporal Arteritis 53 0.055
70
LGN002 Legionellosis 53 0.055
71
P NPH012 Nephrotic Syndrome 52 0.055
72
NRM003 Norum Disease 52 0.055
73
RLP001 Relapsing Polychondritis 52 0.055
74
PRS047 Prostatitis 50 0.055
75
P ABD003 Abdominal Aortic Aneurysm 50 0.055
76
MCR088 Microscopic Polyangiitis 49 0.055
77
P PLY017 Polyarteritis Nodosa 49 0.055
78
P NPH009 Nephrolithiasis 48 0.055
79
THR013 Thoracic Outlet Syndrome 47 0.055
80
BLD044 Bladder Disease 47 0.055
81
PLS011 Plasmacytoma 46 0.055
82
c ART101 Aortic Valve Disease 2 46 0.055
83
MYC002 Mycobacterium Avium Complex Disease 46 0.055
84
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.055
85
VGN023 Vaginitis 44 0.055
86
FCT013 Factor V Leiden Thrombophilia 43 0.055
87
c GCH017 Gaucher Disease, Type Iii 43 0.055
88
P PTS002 Ptosis 42 0.055
89
P TRC086 Trichohepatoenteric Syndrome 1 42 0.055
90
IGG001 Iga Glomerulonephritis 40 0.055
91
MMB002 Membranous Glomerulonephritis 40 0.055
92
ANG018 Angiomyolipoma 40 0.055
93
PRS055 Pierson Syndrome 39 0.055
94
HYP005 Hypokalemia 39 0.055
95
ACT100 Acute Febrile Neutrophilic Dermatosis 38 0.055
96
RTR011 Retroperitoneal Fibrosis 38 0.055
97
CHR564 Chronic Mucocutaneous Candidosis 37 0.055
98
c CNG029 Congenital Mesoblastic Nephroma 35 0.055
99
SPL018 Splenomegaly 34 0.055
100
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.055
101
MJD001 Majeed Syndrome 33 0.055
102
RVL002 Ruvalcaba Syndrome 33 0.055
103
MRB001 Marburg Hemorrhagic Fever 31 0.055
104
P ATX010 Ataxia Neuropathy Spectrum 31 0.055
105
MLK004 Malakoplakia 30 0.055
106
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 30 0.055
107
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 30 0.055
108
SML031 Small Cell Carcinoma of the Bladder 29 0.055
109
HMR023 Hemorrhagic Cystitis 27 0.055
110
c GLM039 Glomerulosclerosis, Focal Segmental, 6 24 0.055
111
P IGN003 Iga Nephropathy 1 24 0.055
112
IMM073 Immunoglobulin a Vasculitis 24 0.055
113
c BNG076 Benign Exophthalmos Syndrome 21 0.055
114
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 19 0.055
115
AND005 Androgen Insensitivity Syndrome, Mild 19 0.055
116
c GLM014 Glomerulopathy with Fibronectin Deposits 1 16 0.055
117
NPH024 Nephrosis Deafness Urinary Tract Digital Malformation 16 0.055
118
TRN046 Transverse Vaginal Septum 16 0.055
119
ANG062 Angioosteohypertrophic Syndrome 16 0.055
120
P CNG326 Congenital Primary Megaureter 14 0.055
121
P RHM011 Rheumatoid Arthritis 88 0.039
122
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.039
123
P RNL014 Renal Cell Carcinoma 81 0.039
124
WLS001 Wilson Disease 74 0.039
125
P NRB001 Neuroblastoma 73 0.039
126
SCK003 Sickle Cell Anemia 71 0.039
127
P SCL016 Scleroderma 69 0.039
128
P FML161 Familial Mediterranean Fever, Ar 67 0.039
129
P FCL005 Focal Segmental Glomerulosclerosis 65 0.039
130
c HMP004 Hemophilia B 65 0.039
131
GLN010 Glanzmann Thrombasthenia 65 0.039
132
c HMP029 Hemophilia a 64 0.039
133
P PRM002 Primary Hyperoxaluria 64 0.039
134
c JVN010 Juvenile Rheumatoid Arthritis 64 0.039
135
P HRM001 Hermansky-Pudlak Syndrome 62 0.039
136
P ART022 Arthritis 61 0.039
137
P PLY014 Polycystic Kidney Disease 60 0.039
138
c PNC108 Pancreatitis, Hereditary 59 0.039
139
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.039
140
P HPT021 Hepatitis 58 0.039
141
CNG368 Congenital Adrenal Hyperplasia 58 0.039
142
P RSP003 Respiratory Failure 58 0.039
143
P DNT015 Dent Disease 57 0.039
144
SRC014 Sarcoma 57 0.039
145
LWS003 Lowe Syndrome 56 0.039
146
ART005 Arteriovenous Malformation 56 0.039
147
CLB001 Coloboma 55 0.039
148
P HMN010 Hemangioma 54 0.039
149
P GLB002 Glioblastoma 53 0.039
150
ORT008 Orotic Aciduria 53 0.039
151
GLB015 Glioblastoma Multiforme 52 0.039
152
P MTH008 Methylmalonic Acidemia 52 0.039
153
P HML002 Hemolytic Anemia 52 0.039
154
P HYP620 Hypoprothrombinemia 52 0.039
155
HNT002 Hantavirus Pulmonary Syndrome 52 0.039
156
END030 End Stage Renal Failure 51 0.039
157
DSM004 Desmoid Tumor 50 0.039
158
P THR014 Thrombocytopenia 50 0.039
159
P SML001 Small Cell Carcinoma 49 0.039
160
SNS001 Sensorineural Hearing Loss 49 0.039
161
c ACT073 Acute Leukemia 49 0.039
162
P THY032 Thyroiditis 48 0.039
163
P SZR006 Seizure Disorder 48 0.039
164
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 48 0.039
165
P CYS036 Cystinosis, Nephropathic 48 0.039
166
PRP030 Purpura 47 0.039
167
NRG002 Neurogenic Bladder 47 0.039
168
GNR005 Gonorrhea 47 0.039
169
P FNC004 Fanconi Syndrome 46 0.039
170
LYM022 Lymphangioma 46 0.039
171
EVN001 Evans' Syndrome 46 0.039
172
P PRT013 Portal Hypertension 45 0.039
173
CLF001 Cleft Lip 45 0.039
174
OCL005 Oculocerebrorenal Syndrome 45 0.039
175
GST045 Gastroenteritis 45 0.039
176
P PLM085 Pulmonary Hemosiderosis 44 0.039
177
CLN003 Clonorchiasis 44 0.039
178
CHR285 Chronic Myelomonocytic Leukemia 44 0.039
179
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 44 0.039
180
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 44 0.039
181
P EXP004 Exophthalmos 44 0.039
182
TRC012 Trichuriasis 44 0.039
183
c PST041 Posterior Urethral Valves 43 0.039
184
P END033 Endocarditis 43 0.039
185
c PND001 Pain Disorder 43 0.039
186
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.039
187
GRN039 Greenberg Skeletal Dysplasia 43 0.039
188
ANR004 Anuria 43 0.039
189
P GLM040 Glioma Susceptibility 1 43 0.039
190
P TRM003 Tremor 43 0.039
191
P AMY082 Amyloidosis, Familial Visceral 43 0.039
192
PPL002 Papillary Carcinoma 43 0.039
193
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 43 0.039
194
RTN023 Retinitis 43 0.039
195
P PYL005 Pyelonephritis 42 0.039
196
FBR032 Fibromuscular Dysplasia 42 0.039
197
FCT001 Factor Viii Deficiency 42 0.039
198
HNC001 Henoch-Schoenlein Purpura 41 0.039
199
PRS042 Prostate Disease 41 0.039
200
MCN001 Mucinous Adenocarcinoma 41 0.039
201
HMS001 Hemosiderosis 40 0.039
202
c HYP617 Hyperoxaluria, Primary, Type 1 40 0.039
203
EXT010 Extramedullary Plasmacytoma 40 0.039
204
ASC002 Ascariasis 39 0.039
205
HMG002 Hemoglobinuria 39 0.039
206
MNN014 Mononeuritis 39 0.039
207
INT017 Intestinal Schistosomiasis 39 0.039
208
MSN001 Mesangial Proliferative Glomerulonephritis 39 0.039
209
CRY021 Cryoglobulinemic Vasculitis 38 0.039
210
GNG002 Ganglioneuroma 38 0.039
211
CLL002 Collecting Duct Carcinoma 38 0.039
212
c ACT042 Acute Pyelonephritis 38 0.039
213
ANH002 Anhidrosis 38 0.039
214
NPH010 Nephrosclerosis 38 0.039
215
GLM011 Glomerulosclerosis 38 0.039
216
HRM002 Hermaphroditism 37 0.039
217
c ACQ014 Acquired Hemophilia 37 0.039
218
CTN013 Cutaneous Anthrax 36 0.039
219
c HMG001 Hemoglobin C Disease 36 0.039
220
P PRL003 Proliferative Glomerulonephritis 36 0.039
221
SCR015 Scarlet Fever 36 0.039
222
FCH003 Fechtner Syndrome 36 0.039
223
EPS006 Epstein Syndrome 36 0.039
224
c ACT068 Acute Cystitis 36 0.039
225
THR035 Thrombasthenia 36 0.039
226
VSC047 Vascular Malformation 35 0.039
227
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 35 0.039
228
DNS007 Dense Deposit Disease 35 0.039
229
TBL003 Tubular Adenocarcinoma 34 0.039
230
PYL004 Pyelitis 34 0.039
231
P ART084 Arteriovenous Fistula 34 0.039
232
ATS010 Autosomal Recessive Disease 33 0.039
233
c ACQ042 Acquired Hemophilia a 33 0.039
234
c SBC003 Subacute Bacterial Endocarditis 33 0.039
235
URT020 Ureterocele 32 0.039
236
c HYP602 Hyperoxaluria, Primary, Type Ii 32 0.039
237
P GLM044 Glomerular Disease 32 0.039
238
c HML032 Hemolytic Uremic Syndrome, Atypical 4 31 0.039
239
ACT040 Acute Poststreptococcal Glomerulonephritis 31 0.039
240
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.039
241
ANG037 Angiomatosis 30 0.039
242
P HYP111 Hyperprolinemia 30 0.039
243
HRS011 Horseshoe Kidney 29 0.039
244
PLV001 Pelvic Lipomatosis 29 0.039
245
P HYP534 Hypomagnesemia 3, Renal 27 0.039
246
c HYP603 Hyperoxaluria, Primary, Type Iii 27 0.039
247
URT036 Urethral Obstruction 26 0.039
248
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 26 0.039
249
c HML034 Hemolytic Uremic Syndrome, Atypical 3 26 0.039
250
GNT004 Gnathomiasis 25 0.039
251
c HML037 Hemolytic Uremic Syndrome, Atypical 5 25 0.039
252
c HML036 Hemolytic Uremic Syndrome, Atypical 6 25 0.039
253
HMX002 Heme Oxygenase-1 Deficiency 25 0.039
254
c HML035 Hemolytic Uremic Syndrome, Atypical 2 24 0.039
255
INT258 Interstitial Nephritis, Karyomegalic 24 0.039
256
MLR007 Male Reproductive System Disease 23 0.039
257
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 23 0.039
258
c GLY017 Glycogen Storage Disease Ic 22 0.039
259
c NPH046 Nephrolithiasis, Type I 22 0.039
260
c GLM027 Glomerulosclerosis, Focal Segmental, 3 22 0.039
261
VSC008 Vascular Hemostatic Disease 22 0.039
262
URC005 Urachal Cyst 21 0.039
263
IMM053 Immunotactoid Glomerulopathy 21 0.039
264
HGH021 Hughes-Stovin Syndrome 21 0.039
265
P C1Q005 C1q Nephropathy 20 0.039
266
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 20 0.039
267
RNL089 Renal Nutcracker Syndrome 20 0.039
268
GLN006 Glandular Cystitis 20 0.039
269
MYH002 Myh9-Related Disorders 19 0.039
270
FBR085 Fibrillary Glomerulonephritis 18 0.039
271
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 18 0.039
272
HYP656 Hypoparathyroidism - Deafness - Renal Disease 18 0.039
273
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 18 0.039
274
FML277 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis with Severe Ocular Involvement 17 0.039
275
DFN256 Deafness and Myopia 17 0.039
276
HYD031 Hydroxyprolinemia 15 0.039
277
URC004 Urachal Cancer 12 0.039
278
DYS034 Dyschondrosteosis Nephritis 11 0.039
279
UVL007 Uveal Coloboma - Cleft Lip and Palate - Intellectual Disability 11 0.039
280
SLC010 Salcedo Syndrome 10 0.039
281
GLM035 Glomerulonephritis - Sparse Hair - Telangiectasis 10 0.039
282
IMM051 Immunotactoid or Fibrillary Glomerulopathy 9 0.039
283
INF059 Infundibulopelvic Dysgenesis 7 0.039
284
THR040 Thrombocytopenia with Elevated Serum Iga and Renal Disease 6 0.039
285
MLG085 Male Genital Disorders 4 0.039