Search results for nephrosis

206 hits were found for nephrosis

# Family MCID Name MIFTS Score
1
P GLL032 Galloway-Mowat Syndrome 45 4.928
2
LPD004 Lipoid Nephrosis 46 4.812
3
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 51 4.565
4
NPH082 Nephrosis with Deafness and Urinary Tract and Digital Malformations 16 4.535
5
c NPH055 Nephrotic Syndrome, Type 1 46 4.519
6
c GLL038 Galloway-Mowat Syndrome 1 37 4.009
7
PRS055 Pierson Syndrome 43 3.517
8
CNG116 Congenital Nephrotic Syndrome Finnish Type 15 3.472
9
c FML015 Familial Nephrotic Syndrome 34 2.863
10
P NPH012 Nephrotic Syndrome 60 2.247
11
PLM171 Pulmonic Stenosis and Congenital Nephrosis 3 2.069
12
VNT030 Ventriculomegaly with Cystic Kidney Disease 22 2.041
13
c FCL082 Focal Segmental Glomerulosclerosis 4 22 2.005
14
DNT019 Daentl Towsend Siegel Syndrome 9 2.005
15
P GLM007 Glomerulonephritis 61 0.159
16
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.146
17
P FCL005 Focal Segmental Glomerulosclerosis 60 0.140
18
END072 Endotheliitis 46 0.140
19
P HPT021 Hepatitis 75 0.133
20
c BLD140 Blood Group, I System 37 0.133
21
AGN016 Aging 65 0.125
22
P HYP086 Hypothyroidism 62 0.108
23
ALP072 Alpha-Fetoprotein Deficiency 32 0.108
24
THR024 Thrombosis 61 0.099
25
P MMB011 Membranous Nephropathy 55 0.099
26
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.099
27
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.099
28
PRT036 Peritonitis 67 0.088
29
INT067 Interstitial Nephritis 51 0.088
30
ANR004 Anuria 49 0.088
31
HMG010 Hemoglobinemia 29 0.088
32
P LKM002 Leukemia 75 0.077
33
P KDN018 Kidney Disease 69 0.077
34
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.077
35
CRB009 Cerebritis 41 0.077
36
MCR067 Microcoria, Congenital 23 0.077
37
c CHR089 Chronic Kidney Failure 72 0.062
38
BRN024 Bronchitis 67 0.062
39
P LYM026 Lymphoblastic Leukemia 66 0.062
40
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.062
41
P PLY018 Polycythemia 60 0.062
42
PRS047 Prostatitis 59 0.062
43
ALL026 Allergic Hypersensitivity Disease 59 0.062
44
P PLY041 Polymyositis 57 0.062
45
NLP001 Nail-Patella Syndrome 56 0.062
46
URM002 Uremia 52 0.062
47
CHN070 Cohen-Gibson Syndrome 51 0.062
48
NPH010 Nephrosclerosis 46 0.062
49
c CHR020 Chronic Interstitial Cystitis 44 0.062
50
CRS001 Crescentic Glomerulonephritis 44 0.062
51
NRN002 Neuronitis 43 0.062
52
AMN006 Aminoaciduria 41 0.062
53
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.062
54
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.062
55
DFF015 Diffuse Glomerulonephritis 32 0.062
56
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.044
57
MYL069 Myeloma, Multiple 86 0.044
58
CRH001 Crohn's Disease 80 0.044
59
P OST002 Osteoporosis 75 0.044
60
ALP046 Alport Syndrome, X-Linked 74 0.044
61
KWS002 Kawasaki Disease 72 0.044
62
VSC007 Vascular Disease 71 0.044
63
P LYM118 Lymphoma 71 0.044
64
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 70 0.044
65
P MYP004 Myopathy 69 0.044
66
P AMY004 Amyloidosis 69 0.044
67
P ANR048 Aniridia 1 68 0.044
68
c HMP004 Hemophilia B 67 0.044
69
DRM006 Dermatitis 67 0.044
70
VSC011 Vasculitis 66 0.044
71
ISC004 Ischemia 66 0.044
72
ACQ007 Acquired Immunodeficiency Syndrome 65 0.044
73
P PSR002 Psoriasis 65 0.044
74
c PRC016 Pre-Eclampsia 65 0.044
75
c CHR417 Chronic Graft Versus Host Disease 65 0.044
76
TTN003 Tetanus 65 0.044
77
P THR014 Thrombocytopenia 65 0.044
78
P CCK001 Cockayne Syndrome 64 0.044
79
P PNC044 Pancreatitis 64 0.044
80
RSP006 Respiratory System Disease 63 0.044
81
P NRP001 Neuropathy 63 0.044
82
ALC006 Alcoholic Hepatitis 62 0.044
83
P HML002 Hemolytic Anemia 62 0.044
84
c CNG006 Congenital Hypothyroidism 62 0.044
85
DFC004 Deficiency Anemia 62 0.044
86
SCH014 Schistosomiasis 62 0.044
87
P HMP007 Hemophilia 61 0.044
88
PLM070 Pulmonic Stenosis 61 0.044
89
P PLY014 Polycystic Kidney Disease 60 0.044
90
P HYP040 Hypospadias 60 0.044
91
CHR177 Chromophobe Renal Cell Carcinoma 59 0.044
92
END030 End Stage Renal Failure 59 0.044
93
P ENC018 Encephalopathy 58 0.044
94
URN009 Urinary System Disease 58 0.044
95
P PLY006 Polydactyly 57 0.044
96
P ECL001 Eclampsia 57 0.044
97
URN010 Urinary Tract Obstruction 57 0.044
98
FCL009 Focal Dermal Hypoplasia 57 0.044
99
IMM136 Immune System Disease 57 0.044
100
CYT008 Cytomegalovirus Infection 57 0.044
101
EXT034 Extrinsic Allergic Alveolitis 57 0.044
102
P PYL005 Pyelonephritis 56 0.044
103
RDC002 Radiculopathy 55 0.044
104
FDL002 Food Allergy 55 0.044
105
CYS010 Cystinosis 55 0.044
106
TCK001 Tick-Borne Encephalitis 55 0.044
107
c MCR113 Microvascular Complications of Diabetes 3 55 0.044
108
P SYP003 Syphilis 55 0.044
109
TRY001 Trypanosomiasis 55 0.044
110
STR008 Strongyloidiasis 54 0.044
111
P ICH004 Ichthyosis 54 0.044
112
P FNC004 Fanconi Syndrome 54 0.044
113
DNY001 Denys-Drash Syndrome 54 0.044
114
c SVR005 Severe Pre-Eclampsia 53 0.044
115
YLL001 Yellow Nail Syndrome 53 0.044
116
PRT038 Protein-Energy Malnutrition 52 0.044
117
STM007 Stomatitis 52 0.044
118
IGG001 Iga Glomerulonephritis 52 0.044
119
HPT082 Hepatic Adenomas, Familial 52 0.044
120
PRR002 Pure Red-Cell Aplasia 52 0.044
121
VRC001 Varicocele 52 0.044
122
PRN021 Paranasal Sinus Disease 51 0.044
123
INT051 Intussusception 51 0.044
124
MMB001 Membranoproliferative Glomerulonephritis 51 0.044
125
FRS002 Frasier Syndrome 51 0.044
126
NSD001 Nose Disease 51 0.044
127
c NGH026 Night Blindness, Congenital Stationary, Type 1a 51 0.044
128
SPR010 Sporotrichosis 50 0.044
129
P HML001 Hemolytic-Uremic Syndrome 50 0.044
130
TRC012 Trichuriasis 50 0.044
131
HYD002 Hydronephrosis 49 0.044
132
P RNL017 Renal Oncocytoma 49 0.044
133
PLL012 Pollen Allergy 48 0.044
134
c ACT042 Acute Pyelonephritis 48 0.044
135
PNT038 Peanut Allergy 48 0.044
136
ISC002 Ischemic Optic Neuropathy 48 0.044
137
c BRN108 Branchiootic Syndrome 1 47 0.044
138
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.044
139
PST011 Pustulosis of Palm and Sole 47 0.044
140
PRT014 Protein S Deficiency 47 0.044
141
CYS036 Cystinosis, Nephropathic 47 0.044
142
MLK006 Milk Allergy 46 0.044
143
NNS002 Nonspecific Interstitial Pneumonia 46 0.044
144
VTM002 Vitamin B12 Deficiency 46 0.044
145
MCL075 Macular Dystrophy, Corneal 46 0.044
146
IMM154 Immunoglobulin a Deficiency 1 45 0.044
147
P PRT026 Parotitis 45 0.044
148
PRS034 Parasitic Helminthiasis Infectious Disease 45 0.044
149
P ANL018 Analbuminemia 45 0.044
150
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.044
151
ASP004 Asphyxia Neonatorum 44 0.044
152
SLR001 Sialuria 44 0.044
153
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 44 0.044
154
DYS015 Dysentery 43 0.044
155
KWS001 Kwashiorkor 43 0.044
156
CWM001 Cow Milk Allergy 42 0.044
157
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.044
158
CMP009 Complement Deficiency 41 0.044
159
c SCN006 Secondary Syphilis 40 0.044
160
PRT019 Protein-Losing Enteropathy 40 0.044
161
CRN286 Corneal Dystrophy, Meesmann 39 0.044
162
MRS001 Marasmus 39 0.044
163
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.044
164
PCH002 Pachygyria 38 0.044
165
RTC003 Root Caries 38 0.044
166
c HYD060 Hydrocephalus, Nonsyndromic, Autosomal Recessive 1 38 0.044
167
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.044
168
BTL002 Beta-Lactam Allergy 37 0.044
169
IRT001 Iritis 36 0.044
170
OCH001 Ochronosis 36 0.044
171
DFF021 Diffuse Mesangial Sclerosis 36 0.044
172
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.044
173
c HYD043 Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 36 0.044
174
HYP114 Hypertensive Nephropathy 35 0.044
175
ACT003 Acute Kidney Tubular Necrosis 34 0.044
176
HYP034 Hypertensive Encephalopathy 34 0.044
177
PRN007 Perinephritis 34 0.044
178
SPN331 Spondyloocular Syndrome 34 0.044
179
APP016 Apple Allergy 33 0.044
180
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.044
181
INF159 Infantile Sialic Acid Storage Disease 33 0.044
182
PRG023 Progeroid Short Stature with Pigmented Nevi 32 0.044
183
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.044
184
c ATR022 Atrial Septal Defect 3 29 0.044
185
ORT001 Orthostatic Proteinuria 29 0.044
186
ASC001 Ascaridiasis 29 0.044
187
EXF003 Exfoliative Dermatitis 28 0.044
188
MTP028 Metaphyseal Dysplasia, Spahr Type 28 0.044
189
KDN013 Kidney Hypertrophy 25 0.044
190
XP2002 Xp22.13p22.2 Duplication Syndrome 23 0.044
191
CRK001 Cork-Handlers' Disease 22 0.044
192
ANR038 Anorexia Nervosa 1 21 0.044
193
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.044
194
c DRM055 Dermatitis, Atopic, 3 21 0.044
195
c NPH070 Nephrotic Syndrome, Type 6 20 0.044
196
XQ1001 Xq12-Q13.3 Duplication Syndrome 20 0.044
197
OST007 Ostertagiasis 20 0.044
198
c FML268 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes 18 0.044
199
BLD137 Blood Group--Ahonen 17 0.044
200
IMM162 Immunoglobulin E Concentration, Serum 16 0.044
201
NPH097 Nephrosialidosis 16 0.044
202
c ATM087 Autoimmune Lymphoproliferative Syndrome Due to Ctla4 Haploinsuffiency 15 0.044
203
CMB082 Combined Oxidative Phosphorylation Deficiency 33 14 0.044
204
SPR076 Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis 14 0.044
205
NPH026 Nephrotic Syndrome, Idiopathic, Steroid-Resistant 11 0.044
206
MSN012 Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities 10 0.044
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