Search results for "hematuria"

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

246 hits were found for 'hematuria'

# Family MCID Name MIFTS Score
1
THN006 Thin Basement Membrane Nephropathy 45 6.115
2
P ALP004 Alport Syndrome 63 5.695
3
LNP001 Loin Pain Hematuria Syndrome 13 4.286
4
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 30 3.235
5
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 1 3.235
6
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 25 2.303
7
CLB014 Coloboma, Cleft Lip/palate and Mental Retardation Syndrome 8 2.269
8
PRT039 Proteinuria 57 0.178
9
SCH014 Schistosomiasis 72 0.135
10
KLP002 Klippel-Trenaunay Syndrome 69 0.122
11
P HYP075 Hypertension 85 0.108
12
URN003 Urinary Schistosomiasis 58 0.108
13
P GLM007 Glomerulonephritis 68 0.091
14
NPH051 Nephritis 53 0.091
15
P GLM015 Glomerulopathy with Fibronectin Deposits 2 24 0.091
16
P GCH001 Gaucher's Disease 83 0.082
17
ADN018 Adenoma 65 0.082
18
TRN018 Transitional Cell Carcinoma 63 0.082
19
NPH001 Nephrogenic Adenoma 43 0.082
20
PYR004 Pyuria 28 0.082
21
TBR010 Tuberculosis 85 0.071
22
P WGN002 Wegener's Granulomatosis 73 0.071
23
NLP001 Nail-Patella Syndrome 70 0.071
24
ART016 Aortic Aneurysm 70 0.071
25
c HMP007 Hemophilia 64 0.071
26
c MLG069 Malignant Hypertension 63 0.071
27
PRS047 Prostatitis 59 0.071
28
P ADN016 Adenocarcinoma 58 0.071
29
c CTR002 Cataract 57 0.071
30
GDP001 Goodpasture Syndrome 54 0.071
31
IGG001 Iga Glomerulonephritis 53 0.071
32
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 0.071
33
P CYS018 Cystitis 51 0.071
34
HMG005 Hemoglobinopathy 51 0.071
35
CRY021 Cryoglobulinemic Vasculitis 49 0.071
36
ANR040 Aneurysm 45 0.071
37
INT067 Interstitial Nephritis 45 0.071
38
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 39 0.071
39
RNL012 Renal Tuberculosis 35 0.071
40
BRR005 Barraquer-Simons Syndrome 34 0.071
41
HRD052 Hereditary Mucoepithelial Dysplasia 27 0.071
42
NPH008 Nephrogenic Adenoma of the Urethra 24 0.071
43
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 17 0.071
44
FBR012 Fabry Disease 85 0.058
45
LSC001 Lesch-Nyhan Syndrome 78 0.058
46
P LKM002 Leukemia 76 0.058
47
CYS013 Cystinuria 76 0.058
48
GLN003 Glanzmann's Thrombasthenia 76 0.058
49
P LYM007 Lymphangioleiomyomatosis 74 0.058
50
P AMY004 Amyloidosis 73 0.058
51
RLP001 Relapsing Polychondritis 72 0.058
52
P TMP003 Temporal Arteritis 72 0.058
53
OCL005 Oculocerebrorenal Syndrome 70 0.058
54
P ABD003 Abdominal Aortic Aneurysm 67 0.058
55
c NPH012 Nephrotic Syndrome 67 0.058
56
P WLM002 Wilms Tumor 66 0.058
57
VGN023 Vaginitis 62 0.058
58
P NPH009 Nephrolithiasis 59 0.058
59
ACT100 Acute Febrile Neutrophilic Dermatosis 57 0.058
60
PLS011 Plasmacytoma 56 0.058
61
FSH001 Fish-Eye Disease 56 0.058
62
MCR088 Microscopic Polyangiitis 56 0.058
63
LGN002 Legionellosis 55 0.058
64
c ATS015 Autosomal Dominant Alport Syndrome 54 0.058
65
URT001 Urethritis 54 0.058
66
P EHL009 Ehlers-Danlos Syndrome Type Iv 53 0.058
67
c TLN008 Telangiectasia, Hereditary Hemorrhagic, Type 5 52 0.058
68
c HYD002 Hydronephrosis 52 0.058
69
RTR011 Retroperitoneal Fibrosis 50 0.058
70
c MSB002 Mesoblastic Nephroma 49 0.058
71
HYP005 Hypokalemia 49 0.058
72
P CND028 Candidiasis, Familial, 4, Autosomal Recessive 47 0.058
73
P CNG029 Congenital Mesoblastic Nephroma 47 0.058
74
c ATS018 Autosomal Recessive Alport Syndrome 47 0.058
75
RVL002 Ruvalcaba Syndrome 46 0.058
76
P MYH004 Myh9 Related Thrombocytopenia 46 0.058
77
SPL018 Splenomegaly 46 0.058
78
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.058
79
PRS055 Pierson Syndrome 41 0.058
80
MJD001 Majeed Syndrome 41 0.058
81
RHB022 Rhabdoid Tumors, Somatic 41 0.058
82
LMY003 Leiomyomatosis 39 0.058
83
c GCH005 Gaucher Disease Type 3 39 0.058
84
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.058
85
HMR023 Hemorrhagic Cystitis 38 0.058
86
SML031 Small Cell Carcinoma of the Bladder 36 0.058
87
MLK004 Malakoplakia 35 0.058
88
BRK004 Barakat Syndrome 34 0.058
89
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 34 0.058
90
MRB001 Marburg Hemorrhagic Fever 29 0.058
91
ALP070 Alport Syndrome - Intellectual Disability - Midface Hypoplasia - Elliptocytosis 26 0.058
92
IMM073 Immunoglobulin a Vasculitis 25 0.058
93
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 22 0.058
94
ESN013 Eosinophilic Cystitis 19 0.058
95
c GLM039 Glomerulosclerosis, Focal Segmental, 6 19 0.058
96
NPH024 Nephrosis Deafness Urinary Tract Digital Malformation 19 0.058
97
TRN046 Transverse Vaginal Septum 16 0.058
98
CNG326 Congenital Primary Megaureter 15 0.058
99
DYS034 Dyschondrosteosis Nephritis 15 0.058
100
SLC010 Salcedo Syndrome 14 0.058
101
GLM035 Glomerulonephritis - Sparse Hair - Telangiectasis 13 0.058
102
c TYP009 Type 2 Diabetes Mellitus 100 0.041
103
P RHM011 Rheumatoid Arthritis 94 0.041
104
P LVR011 Liver Cancer 90 0.041
105
P SYS001 Systemic Lupus Erythematosus 89 0.041
106
P ATX002 Ataxia Telangiectasia 87 0.041
107
SCK003 Sickle Cell Anemia 84 0.041
108
WLS001 Wilson Disease 82 0.041
109
VNH001 Von Hippel-Lindau Disease 81 0.041
110
P HMP004 Hemophilia B 80 0.041
111
P MTH008 Methylmalonic Acidemia 79 0.041
112
P HRD008 Hereditary Hemorrhagic Telangiectasia 76 0.041
113
ANK002 Ankylosing Spondylitis 76 0.041
114
c LPS004 Lupus Erythematosus 75 0.041
115
P ART022 Arthritis 74 0.041
116
FCT001 Factor Viii Deficiency 74 0.041
117
c DBT009 Diabetes Mellitus 73 0.041
118
P CNG368 Congenital Adrenal Hyperplasia 72 0.041
119
P FCL005 Focal Segmental Glomerulosclerosis 72 0.041
120
P ANG001 Angelman Syndrome 71 0.041
121
VNW001 Von Willebrand's Disease 71 0.041
122
DBT011 Diabetic Retinopathy 70 0.041
123
P HMN010 Hemangioma 70 0.041
124
P NRB001 Neuroblastoma 70 0.041
125
c THR014 Thrombocytopenia 69 0.041
126
PLY017 Polyarteritis Nodosa 69 0.041
127
SRC014 Sarcoma 68 0.041
128
P RSP003 Respiratory Failure 68 0.041
129
CLB001 Coloboma 68 0.041
130
c JVN010 Juvenile Rheumatoid Arthritis 67 0.041
131
P SYS005 Systemic Scleroderma 66 0.041
132
P PRT013 Portal Hypertension 65 0.041
133
FCT003 Factor X Deficiency 65 0.041
134
c THY032 Thyroiditis 65 0.041
135
PRP030 Purpura 65 0.041
136
c HML002 Hemolytic Anemia 65 0.041
137
ACN002 Acanthosis Nigricans 64 0.041
138
ART019 Aortic Valve Stenosis 63 0.041
139
c HPT021 Hepatitis 63 0.041
140
P RNL014 Renal Cell Carcinoma 63 0.041
141
P NPH021 Nephropathic Cystinosis 62 0.041
142
ART005 Arteriovenous Malformation 62 0.041
143
c KDN018 Kidney Disease 62 0.041
144
c PLY014 Polycystic Kidney Disease 61 0.041
145
FBR032 Fibromuscular Dysplasia 61 0.041
146
P PRT008 Proteus Syndrome 60 0.041
147
P PRM124 Primary Hyperoxaluria Type 1 60 0.041
148
P ORT008 Orotic Aciduria 59 0.041
149
CLF001 Cleft Lip 59 0.041
150
P DNT039 Dent's Disease 59 0.041
151
GNR005 Gonorrhea 59 0.041
152
PPL002 Papillary Carcinoma 58 0.041
153
ANR004 Anuria 58 0.041
154
EXT010 Extramedullary Plasmacytoma 58 0.041
155
ANH002 Anhidrosis 57 0.041
156
HMS001 Hemosiderosis 57 0.041
157
SNS001 Sensorineural Hearing Loss 57 0.041
158
c ACT073 Acute Leukemia 56 0.041
159
P END033 Endocarditis 56 0.041
160
c MNT147 Mental Retardation 56 0.041
161
PST041 Posterior Urethral Valves 55 0.041
162
ART001 Arterial Tortuosity Syndrome 55 0.041
163
CLN003 Clonorchiasis 55 0.041
164
MSN001 Mesangial Proliferative Glomerulonephritis 55 0.041
165
c TRM003 Tremor 55 0.041
166
c CHR285 Chronic Myelomonocytic Leukemia 55 0.041
167
P EXP004 Exophthalmos 54 0.041
168
P PND001 Pain Disorder 54 0.041
169
MCN001 Mucinous Adenocarcinoma 54 0.041
170
P PYL005 Pyelonephritis 54 0.041
171
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 54 0.041
172
RTN023 Retinitis 53 0.041
173
AND003 Andersen-Tawil Syndrome 53 0.041
174
GST045 Gastroenteritis 53 0.041
175
NRG002 Neurogenic Bladder 52 0.041
176
LPS007 Lupus Nephritis 52 0.041
177
MMB002 Membranous Glomerulonephritis 52 0.041
178
c ACQ014 Acquired Hemophilia 51 0.041
179
HMG002 Hemoglobinuria 51 0.041
180
ANG018 Angiomyolipoma 51 0.041
181
NPH010 Nephrosclerosis 51 0.041
182
RHB017 Rhabdoid Tumor 50 0.041
183
P SZR006 Seizure Disorder 50 0.041
184
P FNC004 Fanconi Syndrome 50 0.041
185
ACT040 Acute Poststreptococcal Glomerulonephritis 49 0.041
186
HRM002 Hermaphroditism 48 0.041
187
P HYP111 Hyperprolinemia 47 0.041
188
GLM011 Glomerulosclerosis 47 0.041
189
P ATX010 Ataxia Neuropathy Spectrum 47 0.041
190
P ART084 Arteriovenous Fistula 46 0.041
191
TRC012 Trichuriasis 46 0.041
192
c PRL003 Proliferative Glomerulonephritis 46 0.041
193
P HMR003 Hemorrhagic Disease 45 0.041
194
P FML003 Familial Visceral Amyloidosis 45 0.041
195
EVN001 Evans' Syndrome 45 0.041
196
DNS007 Dense Deposit Disease 45 0.041
197
THR035 Thrombasthenia 44 0.041
198
HRS011 Horseshoe Kidney 44 0.041
199
LNG029 Lung Adenocarcinoma 43 0.041
200
c INF037 Inflammatory Bowel Disease 43 0.041
201
CMP042 Complement Factor H Deficiency 43 0.041
202
PRT012 Prothrombin Deficiency 43 0.041
203
c ACT042 Acute Pyelonephritis 42 0.041
204
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 42 0.041
205
HNC001 Henoch-Schoenlein Purpura 41 0.041
206
URT020 Ureterocele 38 0.041
207
ANG037 Angiomatosis 38 0.041
208
P RNL042 Renal Hypouricemia 37 0.041
209
SCR015 Scarlet Fever 37 0.041
210
PLV001 Pelvic Lipomatosis 35 0.041
211
c SBC003 Subacute Bacterial Endocarditis 35 0.041
212
TBL003 Tubular Adenocarcinoma 35 0.041
213
SYN053 Syndromic Diarrhea 34 0.041
214
INT017 Intestinal Schistosomiasis 33 0.041
215
CTN013 Cutaneous Anthrax 32 0.041
216
BRG002 Berger Disease 31 0.041
217
URT036 Urethral Obstruction 31 0.041
218
HMX002 Heme Oxygenase-1 Deficiency 31 0.041
219
MTH052 Methylmalonic Acidemia and Homocystinuria Cblc Type 30 0.041
220
c HMG001 Hemoglobin C Disease 29 0.041
221
GNT004 Gnathomiasis 26 0.041
222
KRY002 Karyomegalic Interstitial Nephritis 26 0.041
223
XLN127 X-Linked Diffuse Leiomyomatosis - Alport Syndrome 24 0.041
224
PYL004 Pyelitis 23 0.041
225
c HYP534 Hypomagnesemia 3, Renal 22 0.041
226
c BNG076 Benign Exophthalmos Syndrome 22 0.041
227
SCK031 Sickle Cell - Hemoglobin C Disease 21 0.041
228
c GLY017 Glycogen Storage Disease Ic 20 0.041
229
c HML034 Hemolytic Uremic Syndrome, Atypical 3 19 0.041
230
c HML037 Hemolytic Uremic Syndrome, Atypical 5 19 0.041
231
c HML032 Hemolytic Uremic Syndrome, Atypical 4 19 0.041
232
c HML036 Hemolytic Uremic Syndrome, Atypical 6 19 0.041
233
c HML035 Hemolytic Uremic Syndrome, Atypical 2 19 0.041
234
NPH066 Nephropathy Due to Cfhr5 Deficiency 17 0.041
235
MYH002 Myh9-Related Disorders 17 0.041
236
c FCL027 Focal Segmental Glomerulosclerosis 3 17 0.041
237
HYD031 Hydroxyprolinemia 15 0.041
238
URC004 Urachal Cancer 15 0.041
239
ANG027 Angioma Hereditary Neurocutaneous 14 0.041
240
DFN256 Deafness and Myopia 13 0.041
241
c NPH046 Nephrolithiasis, Type I 12 0.041
242
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 12 0.041
243
P ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 11 0.041
244
INF123 Infundibulopelvic Stenosis - Multicystic Kidney 10 0.041
245
GLN006 Glandular Cystitis 9 0.041
246
THR040 Thrombocytopenia with Elevated Serum Iga and Renal Disease 6 0.041