Search results for "hematuria"

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

217 hits were found for 'hematuria'

# Family MCID Name MIFTS Score
1
THN006 Thin Basement Membrane Nephropathy 43 5.967
2
ALP004 Alport Syndrome 60 4.577
3
LNP001 Loin Pain Hematuria Syndrome 14 4.210
4
LMY008 Leiomyomatosis of Esophagus, Cataract and Hematuria 1 3.167
5
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 25 2.255
6
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 20 2.220
7
ANG055 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle 17 2.220
8
CLB014 Coloboma, Cleft Lip/palate and Mental Retardation Syndrome 8 2.220
9
PRT039 Proteinuria 57 0.176
10
SCH014 Schistosomiasis 70 0.142
11
KLP002 Klippel-Trenaunay Syndrome 67 0.113
12
URN003 Urinary Schistosomiasis 57 0.113
13
P GLM007 Glomerulonephritis 68 0.096
14
NPH051 Nephritis 54 0.096
15
P HYP075 Hypertension 85 0.086
16
PYR004 Pyuria 28 0.086
17
TBR010 Tuberculosis 83 0.074
18
ART016 Aortic Aneurysm 70 0.074
19
c HMP007 Hemophilia 67 0.074
20
TRN018 Transitional Cell Carcinoma 63 0.074
21
PRS047 Prostatitis 60 0.074
22
c CTR002 Cataract 57 0.074
23
IGG001 Iga Glomerulonephritis 52 0.074
24
HMG005 Hemoglobinopathy 51 0.074
25
INT067 Interstitial Nephritis 45 0.074
26
ANR040 Aneurysm 44 0.074
27
RNL012 Renal Tuberculosis 36 0.074
28
P HRD008 Hereditary Hemorrhagic Telangiectasia 81 0.061
29
P LKM002 Leukemia 77 0.061
30
GLN003 Glanzmann's Thrombasthenia 73 0.061
31
P WGN002 Wegener's Granulomatosis 71 0.061
32
PLY017 Polyarteritis Nodosa 69 0.061
33
P ABD003 Abdominal Aortic Aneurysm 67 0.061
34
P AMY004 Amyloidosis 67 0.061
35
ADN018 Adenoma 64 0.061
36
VGN023 Vaginitis 62 0.061
37
P ADN016 Adenocarcinoma 58 0.061
38
P NPH009 Nephrolithiasis 57 0.061
39
PLS011 Plasmacytoma 57 0.061
40
URT001 Urethritis 54 0.061
41
c HYD002 Hydronephrosis 53 0.061
42
P CYS018 Cystitis 51 0.061
43
c MSB002 Mesoblastic Nephroma 50 0.061
44
ADN024 Adenine Phosphoribosyltransferase Deficiency 49 0.061
45
c CNG029 Congenital Mesoblastic Nephroma 48 0.061
46
RTR011 Retroperitoneal Fibrosis 48 0.061
47
HYP005 Hypokalemia 47 0.061
48
SPL018 Splenomegaly 46 0.061
49
NPH001 Nephrogenic Adenoma 43 0.061
50
LMY003 Leiomyomatosis 39 0.061
51
CMP042 Complement Factor H Deficiency 35 0.061
52
HMR023 Hemorrhagic Cystitis 35 0.061
53
PNS012 Paine Syndrome 30 0.061
54
NPH008 Nephrogenic Adenoma of the Urethra 24 0.061
55
P GLM015 Glomerulopathy with Fibronectin Deposits 2 23 0.061
56
TRN046 Transverse Vaginal Septum 16 0.061
57
c TYP009 Type 2 Diabetes Mellitus 95 0.043
58
P RHM011 Rheumatoid Arthritis 93 0.043
59
P ATX002 Ataxia Telangiectasia 86 0.043
60
P SYS001 Systemic Lupus Erythematosus 85 0.043
61
FBR012 Fabry Disease 81 0.043
62
VNH001 Von Hippel-Lindau Disease 80 0.043
63
HPT023 Hepatocellular Carcinoma 79 0.043
64
c DBT009 Diabetes Mellitus 78 0.043
65
P MTH008 Methylmalonic Acidemia 77 0.043
66
WLS001 Wilson Disease 77 0.043
67
P HMP004 Hemophilia B 77 0.043
68
P GCH001 Gaucher's Disease 77 0.043
69
LSC001 Lesch-Nyhan Syndrome 77 0.043
70
P ART022 Arthritis 75 0.043
71
CYS013 Cystinuria 75 0.043
72
ANK002 Ankylosing Spondylitis 74 0.043
73
P LYM007 Lymphangioleiomyomatosis 73 0.043
74
c LPS004 Lupus Erythematosus 72 0.043
75
P FCL005 Focal Segmental Glomerulosclerosis 72 0.043
76
P TMP003 Temporal Arteritis 71 0.043
77
DBT011 Diabetic Retinopathy 70 0.043
78
P ANG001 Angelman Syndrome 70 0.043
79
RLP001 Relapsing Polychondritis 70 0.043
80
c THR014 Thrombocytopenia 70 0.043
81
P NRB001 Neuroblastoma 70 0.043
82
P HMN010 Hemangioma 70 0.043
83
FCT001 Factor Viii Deficiency 70 0.043
84
ACN002 Acanthosis Nigricans 69 0.043
85
VNW001 Von Willebrand's Disease 69 0.043
86
NLP001 Nail-Patella Syndrome 69 0.043
87
SRC014 Sarcoma 69 0.043
88
OCL005 Oculocerebrorenal Syndrome 69 0.043
89
P RSP003 Respiratory Failure 68 0.043
90
P HML002 Hemolytic Anemia 66 0.043
91
c NPH012 Nephrotic Syndrome 66 0.043
92
P SYS005 Systemic Scleroderma 66 0.043
93
P CNG368 Congenital Adrenal Hyperplasia 66 0.043
94
c THY032 Thyroiditis 66 0.043
95
c JVN010 Juvenile Rheumatoid Arthritis 65 0.043
96
PRP030 Purpura 64 0.043
97
c HPT021 Hepatitis 64 0.043
98
ART019 Aortic Valve Stenosis 64 0.043
99
CLB001 Coloboma 64 0.043
100
FCT003 Factor X Deficiency 63 0.043
101
c MLG069 Malignant Hypertension 63 0.043
102
P RNL014 Renal Cell Carcinoma 62 0.043
103
c KDN018 Kidney Disease 62 0.043
104
ART005 Arteriovenous Malformation 62 0.043
105
c PLY014 Polycystic Kidney Disease 61 0.043
106
CLF001 Cleft Lip 59 0.043
107
FBR032 Fibromuscular Dysplasia 59 0.043
108
GNR005 Gonorrhea 59 0.043
109
PPL002 Papillary Carcinoma 59 0.043
110
EXT010 Extramedullary Plasmacytoma 58 0.043
111
ANR004 Anuria 57 0.043
112
P PRT008 Proteus Syndrome 57 0.043
113
SNS001 Sensorineural Hearing Loss 57 0.043
114
c ACT073 Acute Leukemia 56 0.043
115
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 56 0.043
116
ACT100 Acute Febrile Neutrophilic Dermatosis 56 0.043
117
P END033 Endocarditis 56 0.043
118
c CHR285 Chronic Myelomonocytic Leukemia 56 0.043
119
FSH001 Fish-Eye Disease 55 0.043
120
MSN001 Mesangial Proliferative Glomerulonephritis 55 0.043
121
c TRM003 Tremor 55 0.043
122
MCR088 Microscopic Polyangiitis 55 0.043
123
HMS001 Hemosiderosis 55 0.043
124
P EXP004 Exophthalmos 54 0.043
125
CLN003 Clonorchiasis 54 0.043
126
MCN001 Mucinous Adenocarcinoma 54 0.043
127
P PYL005 Pyelonephritis 54 0.043
128
ART001 Arterial Tortuosity Syndrome 54 0.043
129
ANH002 Anhidrosis 54 0.043
130
RTN023 Retinitis 53 0.043
131
P EHL009 Ehlers-Danlos Syndrome Type Iv 53 0.043
132
NPH010 Nephrosclerosis 53 0.043
133
GST045 Gastroenteritis 53 0.043
134
AND003 Andersen-Tawil Syndrome 53 0.043
135
GDP001 Goodpasture Syndrome 52 0.043
136
LPS007 Lupus Nephritis 52 0.043
137
HMG002 Hemoglobinuria 52 0.043
138
PST087 Posterior Urethral Valve 52 0.043
139
P ATS015 Autosomal Dominant Alport Syndrome 52 0.043
140
c ACQ014 Acquired Hemophilia 52 0.043
141
MMB002 Membranous Glomerulonephritis 51 0.043
142
MNT147 Mental Retardation 51 0.043
143
ANG018 Angiomyolipoma 51 0.043
144
NRG002 Neurogenic Bladder 51 0.043
145
P CND026 Candidiasis, Familial, 2, Autosomal Recessive 51 0.043
146
RHB017 Rhabdoid Tumor 50 0.043
147
P FNC004 Fanconi Syndrome 49 0.043
148
LGN002 Legionellosis 49 0.043
149
ACT040 Acute Poststreptococcal Glomerulonephritis 49 0.043
150
HRM002 Hermaphroditism 49 0.043
151
PST041 Posterior Urethral Valves 48 0.043
152
P PND001 Pain Disorder 48 0.043
153
EVN001 Evans' Syndrome 46 0.043
154
CRY021 Cryoglobulinemic Vasculitis 46 0.043
155
GLM011 Glomerulosclerosis 46 0.043
156
ASC002 Ascariasis 46 0.043
157
c PRL003 Proliferative Glomerulonephritis 46 0.043
158
P INF037 Inflammatory Bowel Disease 45 0.043
159
RVL002 Ruvalcaba Syndrome 45 0.043
160
P HYP111 Hyperprolinemia 45 0.043
161
TRC012 Trichuriasis 45 0.043
162
THR035 Thrombasthenia 45 0.043
163
HRS011 Horseshoe Kidney 44 0.043
164
c ATS018 Autosomal Recessive Alport Syndrome 44 0.043
165
P SZR006 Seizure Disorder 43 0.043
166
c ACT042 Acute Pyelonephritis 42 0.043
167
DNS007 Dense Deposit Disease 42 0.043
168
HNC001 Henoch-Schoenlein Purpura 41 0.043
169
P ATX010 Ataxia Neuropathy Spectrum 41 0.043
170
RHB022 Rhabdoid Tumors, Somatic 40 0.043
171
PRS055 Pierson Syndrome 40 0.043
172
GCH006 Gaucher Disease Perinatal Lethal 40 0.043
173
MJD001 Majeed Syndrome 40 0.043
174
ANG037 Angiomatosis 38 0.043
175
PRT012 Prothrombin Deficiency 38 0.043
176
P WLM008 Wilms Tumor, Type 1 38 0.043
177
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 37 0.043
178
SCR015 Scarlet Fever 37 0.043
179
c GCH005 Gaucher Disease Type 3 37 0.043
180
ESN020 Eosinophilic Granulomatosis with Polyangiitis 36 0.043
181
URT020 Ureterocele 36 0.043
182
PLV001 Pelvic Lipomatosis 35 0.043
183
c SBC003 Subacute Bacterial Endocarditis 35 0.043
184
P RNL042 Renal Hypouricemia 35 0.043
185
SML031 Small Cell Carcinoma of the Bladder 35 0.043
186
MLK004 Malakoplakia 35 0.043
187
TBL003 Tubular Adenocarcinoma 35 0.043
188
INT017 Intestinal Schistosomiasis 33 0.043
189
BRR005 Barraquer-Simons Syndrome 33 0.043
190
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 33 0.043
191
CTN013 Cutaneous Anthrax 32 0.043
192
BRK004 Barakat Syndrome 32 0.043
193
SYN053 Syndromic Diarrhea 32 0.043
194
P HMR003 Hemorrhagic Disease 32 0.043
195
BRG002 Berger Disease 31 0.043
196
URT036 Urethral Obstruction 31 0.043
197
c HMG001 Hemoglobin C Disease 29 0.043
198
MRB001 Marburg Hemorrhagic Fever 29 0.043
199
GNT004 Gnathomiasis 27 0.043
200
HRD052 Hereditary Mucoepithelial Dysplasia 26 0.043
201
ALP070 Alport Syndrome - Intellectual Disability - Midface Hypoplasia - Elliptocytosis 24 0.043
202
IMM073 Immunoglobulin a Vasculitis 24 0.043
203
c GLM039 Glomerulosclerosis, Focal Segmental, 6 23 0.043
204
PYL004 Pyelitis 23 0.043
205
c BNG076 Benign Exophthalmos Syndrome 22 0.043
206
SCK031 Sickle Cell - Hemoglobin C Disease 22 0.043
207
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 21 0.043
208
ESN013 Eosinophilic Cystitis 19 0.043
209
NPH024 Nephrosis Deafness Urinary Tract Digital Malformation 18 0.043
210
MYH002 Myh9-Related Disorders 17 0.043
211
CNG326 Congenital Primary Megaureter 15 0.043
212
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 14 0.043
213
DYS034 Dyschondrosteosis Nephritis 14 0.043
214
SLC010 Salcedo Syndrome 14 0.043
215
URC004 Urachal Cancer 13 0.043
216
GLM035 Glomerulonephritis - Sparse Hair - Telangiectasis 12 0.043
217
GLN006 Glandular Cystitis 9 0.043