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

245 hits were found for 'hematuria'

# ++ Fam MCID Name MIFTS Score
1
THN006 Thin Basement Membrane Nephropathy 37 5.950
2
ALP004 Alport Syndrome 55 4.583
3
LNP001 Loin Pain Hematuria Syndrome 12 4.185
4
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 0 3.158
5
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 13 2.215
6
c HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 12 2.215
7
P ANG055 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle 11 2.215
8
CLB014 Coloboma, Cleft Lip/palate and Mental Retardation Syndrome 5 2.215
9
P PRT039 Proteinuria 51 0.169
10
PNS012 Paine Syndrome 35 0.158
11
IDP042 Idiopathic Recurrent Stupor 15 0.153
12
SCH014 Schistosomiasis 59 0.136
13
BRG002 Berger Disease 30 0.129
14
NSY001 N Syndrome 57 0.123
15
URN003 Urinary Schistosomiasis 52 0.116
16
KLP002 Klippel-Trenaunay Syndrome 60 0.108
17
ANK002 Ankylosing Spondylitis 75 0.091
18
P GLM007 Glomerulonephritis 60 0.091
19
NPH051 Nephritis 55 0.091
20
ATX002 Ataxia Telangiectasia 81 0.082
21
P HYP075 Hypertension 76 0.082
22
P HMP004 Hemophilia B 66 0.082
23
c CTR002 Cataract 48 0.082
24
FCT013 Factor V Leiden Thrombophilia 31 0.082
25
PYR004 Pyuria 27 0.082
26
TBR010 Tuberculosis 82 0.071
27
RLP001 Relapsing Polychondritis 66 0.071
28
c HMP007 Hemophilia 64 0.071
29
ART016 Aortic Aneurysm 62 0.071
30
TRN018 Transitional Cell Carcinoma 61 0.071
31
EVN001 Evans' Syndrome 50 0.071
32
INT067 Interstitial Nephritis 49 0.071
33
HMG005 Hemoglobinopathy 47 0.071
34
P ATS015 Autosomal Dominant Alport Syndrome 43 0.071
35
ENT001 Enterocele 39 0.071
36
c ATS018 Autosomal Recessive Alport Syndrome 38 0.071
37
RNL012 Renal Tuberculosis 33 0.071
38
c ERL004 Early Yaws 29 0.071
39
RPT003 Ruptured Aortic Aneurysm 22 0.071
40
HRD008 Hereditary Hemorrhagic Telangiectasia 74 0.058
41
ACN002 Acanthosis Nigricans 70 0.058
42
LKM002 Leukemia 70 0.058
43
BLD042 Bladder Carcinoma 70 0.058
44
HPT023 Hepatocellular Carcinoma 69 0.058
45
ADN018 Adenoma 67 0.058
46
P AMY004 Amyloidosis 65 0.058
47
P ABD003 Abdominal Aortic Aneurysm 65 0.058
48
PLY017 Polyarteritis Nodosa 62 0.058
49
P ADN016 Adenocarcinoma 60 0.058
50
P NPH009 Nephrolithiasis 57 0.058
51
PLS011 Plasmacytoma 52 0.058
52
HYP005 Hypokalemia 50 0.058
53
AMY053 Amyloidosis, Secondary 50 0.058
54
SPL018 Splenomegaly 50 0.058
55
P PND001 Pain Disorder 49 0.058
56
c HYD002 Hydronephrosis 48 0.058
57
P CYS018 Cystitis 47 0.058
58
LMY003 Leiomyomatosis 43 0.058
59
c MSB002 Mesoblastic Nephroma 42 0.058
60
RTR011 Retroperitoneal Fibrosis 42 0.058
61
ADN024 Adenine Phosphoribosyltransferase Deficiency 42 0.058
62
RPT002 Ruptured Abdominal Aortic Aneurysm 40 0.058
63
NPH001 Nephrogenic Adenoma 39 0.058
64
c CNG029 Congenital Mesoblastic Nephroma 38 0.058
65
CMP042 Complement Factor H Deficiency 31 0.058
66
P GLM015 Glomerulopathy with Fibronectin Deposits 2 17 0.058
67
TRN046 Transverse Vaginal Septum 13 0.058
68
P SYS001 Systemic Lupus Erythematosus 83 0.041
69
P RHM011 Rheumatoid Arthritis 83 0.041
70
P ART022 Arthritis 75 0.041
71
FBR012 Fabry Disease 74 0.041
72
WLS001 Wilson Disease 74 0.041
73
P GCH001 Gaucher's Disease 73 0.041
74
c DBT009 Diabetes Mellitus 68 0.041
75
GLN003 Glanzmann's Thrombasthenia 68 0.041
76
LSC001 Lesch-Nyhan Syndrome 68 0.041
77
LYM007 Lymphangioleiomyomatosis 67 0.041
78
P WGN002 Wegener's Granulomatosis 67 0.041
79
CYS013 Cystinuria 67 0.041
80
P ANG001 Angelman Syndrome 67 0.041
81
c THR014 Thrombocytopenia 66 0.041
82
DBT011 Diabetic Retinopathy 66 0.041
83
P CNG026 Congenital Heart Defect 65 0.041
84
c LPS004 Lupus Erythematosus 65 0.041
85
c HPT021 Hepatitis 65 0.041
86
P TMP003 Temporal Arteritis 64 0.041
87
ART019 Aortic Valve Stenosis 64 0.041
88
CNG368 Congenital Adrenal Hyperplasia 64 0.041
89
P FCL005 Focal Segmental Glomerulosclerosis 64 0.041
90
WST001 West Syndrome 64 0.041
91
P SYS005 Systemic Scleroderma 63 0.041
92
FCT007 Factor Vii Deficiency 63 0.041
93
c JVN010 Juvenile Rheumatoid Arthritis 62 0.041
94
ACT073 Acute Leukemia 62 0.041
95
P PLY014 Polycystic Kidney Disease 62 0.041
96
ART005 Arteriovenous Malformation 62 0.041
97
P MTH008 Methylmalonic Acidemia 62 0.041
98
HMN010 Hemangioma 62 0.041
99
OCL005 Oculocerebrorenal Syndrome 61 0.041
100
LMY002 Leiomyoma 61 0.041
101
PRP030 Purpura 60 0.041
102
P NRB001 Neuroblastoma 60 0.041
103
PPL002 Papillary Carcinoma 60 0.041
104
HML002 Hemolytic Anemia 60 0.041
105
P RSP003 Respiratory Failure 60 0.041
106
P CLF002 Cleft Palate 60 0.041
107
FCT006 Factor V Deficiency 58 0.041
108
SCK005 Sickle Cell Disease 58 0.041
109
NLP001 Nail-Patella Syndrome 58 0.041
110
MCR088 Microscopic Polyangiitis 58 0.041
111
c NPH012 Nephrotic Syndrome 57 0.041
112
FCL008 Focal Glomerulosclerosis 57 0.041
113
P MMB002 Membranous Glomerulonephritis 56 0.041
114
CLB001 Coloboma 56 0.041
115
FCT001 Factor Viii Deficiency 56 0.041
116
SNS001 Sensorineural Hearing Loss 55 0.041
117
P PRT008 Proteus Syndrome 55 0.041
118
PRX003 Paroxysmal Nocturnal Hemoglobinuria 55 0.041
119
LPS007 Lupus Nephritis 55 0.041
120
SRC014 Sarcoma 54 0.041
121
FBR032 Fibromuscular Dysplasia 54 0.041
122
FCT003 Factor X Deficiency 54 0.041
123
NRG002 Neurogenic Bladder 54 0.041
124
MCN001 Mucinous Adenocarcinoma 54 0.041
125
c MLG069 Malignant Hypertension 53 0.041
126
ANR004 Anuria 53 0.041
127
CHR285 Chronic Myelomonocytic Leukemia 53 0.041
128
NPH010 Nephrosclerosis 53 0.041
129
ANG018 Angiomyolipoma 52 0.041
130
c KDN018 Kidney Disease 52 0.041
131
RNL015 Renal Hypertension 52 0.041
132
P FNC004 Fanconi Syndrome 52 0.041
133
HMG002 Hemoglobinuria 52 0.041
134
P CLL015 Collagen Disease 52 0.041
135
EXT010 Extramedullary Plasmacytoma 52 0.041
136
GNR005 Gonorrhea 52 0.041
137
ART001 Arterial Tortuosity Syndrome 52 0.041
138
GDP001 Goodpasture Syndrome 51 0.041
139
P EXP004 Exophthalmos 51 0.041
140
HMS001 Hemosiderosis 51 0.041
141
RNL014 Renal Cell Carcinoma 51 0.041
142
c MNT147 Mental Retardation 51 0.041
143
P PYL005 Pyelonephritis 51 0.041
144
c TRM003 Tremor 50 0.041
145
ADL002 Adult Syndrome 50 0.041
146
c PRL003 Proliferative Glomerulonephritis 49 0.041
147
PPL020 Papillary Thyroid Carcinoma 49 0.041
148
ACT100 Acute Febrile Neutrophilic Dermatosis 49 0.041
149
RHB017 Rhabdoid Tumor 49 0.041
150
HMR003 Hemorrhagic Disease 49 0.041
151
c ACT042 Acute Pyelonephritis 49 0.041
152
THR035 Thrombasthenia 49 0.041
153
MSN001 Mesangial Proliferative Glomerulonephritis 49 0.041
154
ANH002 Anhidrosis 48 0.041
155
URT010 Ureteral Obstruction 48 0.041
156
PST087 Posterior Urethral Valve 47 0.041
157
LGN002 Legionellosis 47 0.041
158
GST045 Gastroenteritis 46 0.041
159
PRT012 Prothrombin Deficiency 46 0.041
160
CLN003 Clonorchiasis 45 0.041
161
c ACQ014 Acquired Hemophilia 45 0.041
162
P INF037 Inflammatory Bowel Disease 44 0.041
163
ASC002 Ascariasis 44 0.041
164
ACT040 Acute Poststreptococcal Glomerulonephritis 43 0.041
165
RCR001 Recurrent Corneal Erosion 43 0.041
166
HRM002 Hermaphroditism 43 0.041
167
P END033 Endocarditis 42 0.041
168
TRC012 Trichuriasis 42 0.041
169
RVL002 Ruvalcaba Syndrome 42 0.041
170
PST041 Posterior Urethral Valves 42 0.041
171
P CND026 Candidiasis, Familial, 2, Autosomal Recessive 41 0.041
172
CMP009 Complement Deficiency 41 0.041
173
FSH001 Fish-Eye Disease 41 0.041
174
SZR006 Seizure Disorder 40 0.041
175
HRS011 Horseshoe Kidney 39 0.041
176
AND003 Andersen-Tawil Syndrome 39 0.041
177
IGG001 Iga Glomerulonephritis 39 0.041
178
c ATS010 Autosomal Recessive Disease 39 0.041
179
P HYP111 Hyperprolinemia 38 0.041
180
MJD001 Majeed Syndrome 38 0.041
181
MSS002 Mass Syndrome 37 0.041
182
c CTR120 Cataract, Congenital 37 0.041
183
ANG037 Angiomatosis 37 0.041
184
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.041
185
CRY021 Cryoglobulinemic Vasculitis 36 0.041
186
GCH006 Gaucher Disease Perinatal Lethal 35 0.041
187
c SBC003 Subacute Bacterial Endocarditis 35 0.041
188
HNC001 Henoch-Schoenlein Purpura 35 0.041
189
SCR015 Scarlet Fever 34 0.041
190
c ATX010 Ataxia Neuropathy Spectrum 33 0.041
191
NPH016 Nephropathy-Hypertension 33 0.041
192
URT020 Ureterocele 32 0.041
193
BDS002 Bod Syndrome 32 0.041
194
c HRN019 Hair-an Syndrome 32 0.041
195
URT036 Urethral Obstruction 31 0.041
196
TBL003 Tubular Adenocarcinoma 31 0.041
197
MCR029 Micro Syndrome 31 0.041
198
c GCH005 Gaucher Disease Type 3 30 0.041
199
PLV001 Pelvic Lipomatosis 30 0.041
200
P EHL009 Ehlers-Danlos Syndrome Type Iv 30 0.041
201
MLK004 Malakoplakia 30 0.041
202
INT017 Intestinal Schistosomiasis 30 0.041
203
P WLM008 Wilms Tumor, Type 1 29 0.041
204
PRS055 Pierson Syndrome 29 0.041
205
CTN013 Cutaneous Anthrax 28 0.041
206
HMG001 Hemoglobin C Disease 28 0.041
207
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 27 0.041
208
RNL042 Renal Hypouricemia 27 0.041
209
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 27 0.041
210
BRK004 Barakat Syndrome 27 0.041
211
c HMP017 Hemophilia a, Congenital 26 0.041
212
BRR005 Barraquer-Simons Syndrome 26 0.041
213
HMG004 Hemoglobin D Disease 24 0.041
214
MRB001 Marburg Hemorrhagic Fever 24 0.041
215
c GLM039 Glomerulosclerosis, Focal Segmental, 6 24 0.041
216
SML031 Small Cell Carcinoma of the Bladder 23 0.041
217
c HMP016 Hemophilia a, Acquired 22 0.041
218
ALP058 Alport Syndrome - Intellectual Deficit - Midface Hypoplasia - Elliptocytosis 22 0.041
219
ESN020 Eosinophilic Granulomatosis with Polyangiitis 21 0.041
220
GNT004 Gnathomiasis 21 0.041
221
DFF015 Diffuse Glomerulonephritis 21 0.041
222
IMM073 Immunoglobulin a Vasculitis 21 0.041
223
HRD052 Hereditary Mucoepithelial Dysplasia 21 0.041
224
RNL018 Renal Pelvis Carcinoma 19 0.041
225
SCK020 Sickle Cell - Hemoglobin D Disease 19 0.041
226
SCK031 Sickle Cell - Hemoglobin C Disease 19 0.041
227
PYL004 Pyelitis 18 0.041
228
ESN013 Eosinophilic Cystitis 17 0.041
229
c BNG076 Benign Exophthalmos Syndrome 17 0.041
230
c MMB003 Membranoproliferative Glomerulonephritis Type 2 16 0.041
231
MYH002 Myh9-Related Disorders 15 0.041
232
P ACT079 Acute Proliferative Glomerulonephritis 14 0.041
233
PST042 Posterior Valve Urethra 14 0.041
234
GLN006 Glandular Cystitis 13 0.041
235
URT025 Ureter Tuberculosis 13 0.041
236
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 12 0.041
237
NPH024 Nephrosis Deafness Urinary Tract Digital Malformation 12 0.041
238
WSS001 Wissler's Syndrome 11 0.041
239
URC004 Urachal Cancer 11 0.041
240
CNG326 Congenital Primary Megaureter 10 0.041
241
SLC010 Salcedo Syndrome 10 0.041
242
DYS034 Dyschondrosteosis Nephritis 9 0.041
243
GLM035 Glomerulonephritis - Sparse Hair - Telangiectasis 9 0.041
244
c DMN008 Dominant Cleft Palate 8 0.041
245
UVL005 Uveal Coloboma - Cleft Lip and Palate - Intellectual Deficit 8 0.041