Search results for "hematuria"

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

252 hits were found for 'hematuria'

# Family MCID Name MIFTS Score
1
HMT008 Hematuria, Benign Familial 28 6.809
2
P ALP004 Alport Syndrome 60 4.667
3
LNP001 Loin Pain Hematuria Syndrome 11 4.257
4
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 26 3.925
5
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 1 3.234
6
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 21 2.312
7
CLB014 Coloboma, Cleft Lip/palate and Mental Retardation Syndrome 7 2.254
8
PRT039 Proteinuria 43 0.178
9
SCH014 Schistosomiasis 60 0.132
10
URN003 Urinary Schistosomiasis 50 0.106
11
NPH051 Nephritis 46 0.098
12
P GLM007 Glomerulonephritis 59 0.089
13
PYR004 Pyuria 24 0.089
14
ADN018 Adenoma 55 0.080
15
TRN018 Transitional Cell Carcinoma 54 0.080
16
P CYS018 Cystitis 43 0.080
17
NPH001 Nephrogenic Adenoma 36 0.080
18
P GLM015 Glomerulopathy with Fibronectin Deposits 2 20 0.080
19
P HRD008 Hereditary Hemorrhagic Telangiectasia 75 0.069
20
TBR010 Tuberculosis 73 0.069
21
ART016 Aortic Aneurysm 62 0.069
22
NLP001 Nail-Patella Syndrome 61 0.069
23
P HMP007 Hemophilia 59 0.069
24
P RHB017 Rhabdoid Tumor 54 0.069
25
c MLG069 Malignant Hypertension 54 0.069
26
PRS047 Prostatitis 51 0.069
27
P CTR002 Cataract 50 0.069
28
P ADN016 Adenocarcinoma 49 0.069
29
IGG001 Iga Glomerulonephritis 46 0.069
30
GDP001 Goodpasture Syndrome 46 0.069
31
ADN024 Adenine Phosphoribosyltransferase Deficiency 45 0.069
32
HNC001 Henoch-Schoenlein Purpura 44 0.069
33
HMG005 Hemoglobinopathy 44 0.069
34
c ALP073 Alport Syndrome, Autosomal Recessive 40 0.069
35
INT067 Interstitial Nephritis 38 0.069
36
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.069
37
ANR040 Aneurysm 35 0.069
38
c ALP074 Alport Syndrome, Autosomal Dominant 34 0.069
39
RNL012 Renal Tuberculosis 30 0.069
40
c LPD019 Lipodystrophy, Partial, Acquired 27 0.069
41
CMP042 Complement Factor H Deficiency 26 0.069
42
NPH008 Nephrogenic Adenoma of the Urethra 20 0.069
43
ESN013 Eosinophilic Cystitis 16 0.069
44
c SYS001 Systemic Lupus Erythematosus 91 0.056
45
FBR012 Fabry Disease 76 0.056
46
P GCH001 Gaucher's Disease 70 0.056
47
LSC001 Lesch-Nyhan Syndrome 69 0.056
48
P LPS004 Lupus Erythematosus 67 0.056
49
P CYS013 Cystinuria 67 0.056
50
P LKM002 Leukemia 66 0.056
51
P ANG001 Angelman Syndrome 66 0.056
52
P LYM007 Lymphangioleiomyomatosis 65 0.056
53
CHR063 Chronic Mucocutaneous Candidiasis 63 0.056
54
P AMY004 Amyloidosis 63 0.056
55
RLP001 Relapsing Polychondritis 63 0.056
56
P WLM002 Wilms Tumor 70 0.056
57
P TMP003 Temporal Arteritis 62 0.056
58
PLY017 Polyarteritis Nodosa 60 0.056
59
P NPH012 Nephrotic Syndrome 60 0.056
60
FCT003 Factor X Deficiency 58 0.056
61
P ABD003 Abdominal Aortic Aneurysm 58 0.056
62
WGN006 Wegener Granulomatosis 57 0.056
63
ACN002 Acanthosis Nigricans 55 0.056
64
P NPH009 Nephrolithiasis 51 0.056
65
OCL005 Oculocerebrorenal Syndrome 51 0.056
66
VGN023 Vaginitis 51 0.056
67
CRY008 Cryopyrin-Associated Periodic Syndrome 50 0.056
68
PLS011 Plasmacytoma 49 0.056
69
c SCN045 Secondary Amyloidosis 50 0.056
70
MCR088 Microscopic Polyangiitis 49 0.056
71
ACT100 Acute Febrile Neutrophilic Dermatosis 48 0.056
72
c SPN225 Spondyloarthropathy 1 48 0.056
73
NRM003 Norum Disease 48 0.056
74
URT001 Urethritis 48 0.056
75
LGN002 Legionellosis 47 0.056
76
c EHL057 Ehlers-Danlos Syndrome, Type Iv 48 0.056
77
P HYD002 Hydronephrosis 45 0.056
78
c GCH015 Gaucher Disease, Type I 46 0.056
79
P MSB002 Mesoblastic Nephroma 42 0.056
80
KLP010 Klippel-Trenaunay-Weber Syndrome 43 0.056
81
HYP005 Hypokalemia 42 0.056
82
c CNG029 Congenital Mesoblastic Nephroma 41 0.056
83
SPL018 Splenomegaly 40 0.056
84
MMB002 Membranous Glomerulonephritis 40 0.056
85
RTR011 Retroperitoneal Fibrosis 39 0.056
86
P TRC086 Trichohepatoenteric Syndrome 1 39 0.056
87
RVL002 Ruvalcaba Syndrome 39 0.056
88
P PTS002 Ptosis 39 0.056
89
PRS055 Pierson Syndrome 36 0.056
90
ESN020 Eosinophilic Granulomatosis with Polyangiitis 35 0.056
91
LMY003 Leiomyomatosis 33 0.056
92
c GCH017 Gaucher Disease, Type Iii 34 0.056
93
HMR023 Hemorrhagic Cystitis 32 0.056
94
c ART101 Aortic Valve Disease 2 32 0.056
95
SML031 Small Cell Carcinoma of the Bladder 32 0.056
96
MJD001 Majeed Syndrome 31 0.056
97
MLK004 Malakoplakia 31 0.056
98
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 31 0.056
99
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 30 0.056
100
MRB001 Marburg Hemorrhagic Fever 31 0.056
101
P ATX010 Ataxia Neuropathy Spectrum 29 0.056
102
P CRY007 Cryoglobulinemia, Familial Mixed 25 0.056
103
ALP070 Alport Syndrome - Intellectual Disability - Midface Hypoplasia - Elliptocytosis 22 0.056
104
HRD052 Hereditary Mucoepithelial Dysplasia 21 0.056
105
c GLM039 Glomerulosclerosis, Focal Segmental, 6 20 0.056
106
c BNG076 Benign Exophthalmos Syndrome 19 0.056
107
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 18 0.056
108
c GLM014 Glomerulopathy with Fibronectin Deposits 1 17 0.056
109
FML277 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis with Severe Ocular Involvement 16 0.056
110
NPH024 Nephrosis Deafness Urinary Tract Digital Malformation 16 0.056
111
ANG062 Angioosteohypertrophic Syndrome 15 0.056
112
TRN046 Transverse Vaginal Septum 15 0.056
113
P CNG326 Congenital Primary Megaureter 14 0.056
114
UVL007 Uveal Coloboma - Cleft Lip and Palate - Intellectual Disability 12 0.056
115
DYS034 Dyschondrosteosis Nephritis 12 0.056
116
SLC010 Salcedo Syndrome 11 0.056
117
HPT023 Hepatocellular Carcinoma 95 0.040
118
P RHM011 Rheumatoid Arthritis 94 0.040
119
P ATX030 Ataxia-Telangiectasia 76 0.040
120
P RNL014 Renal Cell Carcinoma 83 0.040
121
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.040
122
WLS001 Wilson Disease 74 0.040
123
c HMP004 Hemophilia B 72 0.040
124
SCK003 Sickle Cell Anemia 70 0.040
125
P SCL016 Scleroderma 76 0.040
126
P PRM002 Primary Hyperoxaluria 68 0.040
127
P NRB001 Neuroblastoma 68 0.040
128
VNW001 Von Willebrand's Disease 67 0.040
129
P CNG368 Congenital Adrenal Hyperplasia 66 0.040
130
P ART022 Arthritis 65 0.040
131
P MTH008 Methylmalonic Acidemia 63 0.040
132
GLN010 Glanzmann Thrombasthenia 63 0.040
133
P RSP003 Respiratory Failure 62 0.040
134
SRC014 Sarcoma 61 0.040
135
P HMN010 Hemangioma 60 0.040
136
P GLB002 Glioblastoma 59 0.040
137
c JVN010 Juvenile Rheumatoid Arthritis 59 0.040
138
P FCL005 Focal Segmental Glomerulosclerosis 58 0.040
139
P KDN018 Kidney Disease 57 0.040
140
P HML002 Hemolytic Anemia 56 0.040
141
END030 End Stage Renal Failure 56 0.040
142
P THY032 Thyroiditis 56 0.040
143
P THR014 Thrombocytopenia 56 0.040
144
P SZR006 Seizure Disorder 56 0.040
145
P HPT021 Hepatitis 55 0.040
146
P DNT015 Dent Disease 55 0.040
147
ORT008 Orotic Aciduria 54 0.040
148
PRP030 Purpura 54 0.040
149
CLB001 Coloboma 54 0.040
150
P HYP620 Hypoprothrombinemia 54 0.040
151
FBR032 Fibromuscular Dysplasia 53 0.040
152
ART005 Arteriovenous Malformation 53 0.040
153
P PLY014 Polycystic Kidney Disease 53 0.040
154
P AND016 Andersen Syndrome 54 0.040
155
MYC002 Mycobacterium Avium Complex Disease 51 0.040
156
CLF001 Cleft Lip 51 0.040
157
FCT001 Factor Viii Deficiency 51 0.040
158
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 51 0.040
159
GLB015 Glioblastoma Multiforme 51 0.040
160
GNR005 Gonorrhea 50 0.040
161
PST041 Posterior Urethral Valves 50 0.040
162
EXT010 Extramedullary Plasmacytoma 49 0.040
163
PPL002 Papillary Carcinoma 49 0.040
164
P PRT013 Portal Hypertension 49 0.040
165
ANR004 Anuria 48 0.040
166
ART001 Arterial Tortuosity Syndrome 48 0.040
167
ANH002 Anhidrosis 48 0.040
168
P TRM003 Tremor 48 0.040
169
SNS001 Sensorineural Hearing Loss 48 0.040
170
c CHR285 Chronic Myelomonocytic Leukemia 48 0.040
171
c ACT073 Acute Leukemia 48 0.040
172
P END033 Endocarditis 48 0.040
173
HMS001 Hemosiderosis 47 0.040
174
P EXP004 Exophthalmos 47 0.040
175
P MNT147 Mental Retardation 46 0.040
176
CLN003 Clonorchiasis 46 0.040
177
MSN001 Mesangial Proliferative Glomerulonephritis 46 0.040
178
c PND001 Pain Disorder 46 0.040
179
c ACQ014 Acquired Hemophilia 45 0.040
180
GST045 Gastroenteritis 45 0.040
181
MCN001 Mucinous Adenocarcinoma 45 0.040
182
THR013 Thoracic Outlet Syndrome 45 0.040
183
RTN023 Retinitis 44 0.040
184
P FNC004 Fanconi Syndrome 44 0.040
185
NRG002 Neurogenic Bladder 44 0.040
186
LPS007 Lupus Nephritis 44 0.040
187
HMG002 Hemoglobinuria 43 0.040
188
NPH010 Nephrosclerosis 43 0.040
189
P PYL005 Pyelonephritis 43 0.040
190
ANG018 Angiomyolipoma 43 0.040
191
MNN014 Mononeuritis 43 0.040
192
DNS007 Dense Deposit Disease 42 0.040
193
P AMY082 Amyloidosis, Familial Visceral 43 0.040
194
GNG002 Ganglioneuroma 42 0.040
195
ACT040 Acute Poststreptococcal Glomerulonephritis 41 0.040
196
P ART084 Arteriovenous Fistula 40 0.040
197
GLM011 Glomerulosclerosis 40 0.040
198
HRM002 Hermaphroditism 40 0.040
199
P HMR003 Hemorrhagic Disease 39 0.040
200
ASC002 Ascariasis 39 0.040
201
EVN001 Evans' Syndrome 39 0.040
202
TRC012 Trichuriasis 39 0.040
203
P INF037 Inflammatory Bowel Disease 39 0.040
204
P PRL003 Proliferative Glomerulonephritis 39 0.040
205
HRS011 Horseshoe Kidney 38 0.040
206
FCH003 Fechtner Syndrome 38 0.040
207
P CYS036 Cystinosis, Nephropathic 38 0.040
208
THR035 Thrombasthenia 37 0.040
209
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 38 0.040
210
c ACT042 Acute Pyelonephritis 36 0.040
211
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 35 0.040
212
P HYP111 Hyperprolinemia 34 0.040
213
URT020 Ureterocele 33 0.040
214
ANG037 Angiomatosis 33 0.040
215
c HYP617 Hyperoxaluria, Primary, Type 1 33 0.040
216
SCR015 Scarlet Fever 31 0.040
217
c SBC003 Subacute Bacterial Endocarditis 29 0.040
218
INT017 Intestinal Schistosomiasis 29 0.040
219
PLV001 Pelvic Lipomatosis 29 0.040
220
TBL003 Tubular Adenocarcinoma 29 0.040
221
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 29 0.040
222
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 29 0.040
223
HMX002 Heme Oxygenase-1 Deficiency 28 0.040
224
CTN013 Cutaneous Anthrax 28 0.040
225
EPS006 Epstein Syndrome 28 0.040
226
URT036 Urethral Obstruction 26 0.040
227
BRG002 Berger Disease 26 0.040
228
c HMG001 Hemoglobin C Disease 24 0.040
229
SCK031 Sickle Cell - Hemoglobin C Disease 23 0.040
230
GNT004 Gnathomiasis 22 0.040
231
MMB005 Membranous Glomerulonephritis, Antenatal 21 0.040
232
PYL004 Pyelitis 19 0.040
233
c HML035 Hemolytic Uremic Syndrome, Atypical 2 18 0.040
234
c HML034 Hemolytic Uremic Syndrome, Atypical 3 18 0.040
235
c HML037 Hemolytic Uremic Syndrome, Atypical 5 18 0.040
236
INT258 Interstitial Nephritis, Karyomegalic 19 0.040
237
MYH002 Myh9-Related Disorders 18 0.040
238
c HML032 Hemolytic Uremic Syndrome, Atypical 4 18 0.040
239
c HML036 Hemolytic Uremic Syndrome, Atypical 6 17 0.040
240
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 17 0.040
241
AND005 Androgen Insensitivity Syndrome, Mild 17 0.040
242
c NPH046 Nephrolithiasis, Type I 16 0.040
243
P HYP534 Hypomagnesemia 3, Renal 16 0.040
244
c GLM027 Glomerulosclerosis, Focal Segmental, 3 16 0.040
245
c GLY017 Glycogen Storage Disease Ic 15 0.040
246
HYD031 Hydroxyprolinemia 14 0.040
247
URC004 Urachal Cancer 11 0.040
248
NPH066 Nephropathy Due to Cfhr5 Deficiency 11 0.040
249
DFN256 Deafness and Myopia 10 0.040
250
GLN006 Glandular Cystitis 8 0.040
251
THR040 Thrombocytopenia with Elevated Serum Iga and Renal Disease 6 0.040
252
INF059 Infundibulopelvic Dysgenesis 5 0.040