Search results for nephrosis

105 hits were found for nephrosis

# Family MCID Name MIFTS Score
1
GLL032 Galloway-Mowat Syndrome 51 5.813
2
LPD004 Lipoid Nephrosis 48 5.116
3
NPH082 Nephrosis with Deafness and Urinary Tract and Digital Malformations 12 4.641
4
c NPH055 Nephrotic Syndrome, Type 1 51 4.595
5
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 49 3.639
6
PRS055 Pierson Syndrome 46 3.615
7
CNG116 Congenital Nephrotic Syndrome Finnish Type 28 3.560
8
c FML015 Familial Nephrotic Syndrome 36 2.906
9
P NPH012 Nephrotic Syndrome 59 2.373
10
VNT030 Ventriculomegaly with Cystic Kidney Disease 19 2.101
11
c GLM033 Glomerulosclerosis, Focal Segmental, 4 30 2.055
12
HYP666 Hypoparathyroidism-Deafness-Renal Disease Syndrome 26 2.055
13
DNT019 Daentl Towsend Siegel Syndrome 9 2.055
14
P GLM007 Glomerulonephritis 59 0.199
15
END072 Endotheliitis 42 0.175
16
P HPT021 Hepatitis 69 0.166
17
P FCL005 Focal Segmental Glomerulosclerosis 60 0.166
18
P HYP086 Hypothyroidism 64 0.136
19
THR024 Thrombosis 57 0.124
20
INT067 Interstitial Nephritis 46 0.111
21
ANR004 Anuria 45 0.111
22
HMG010 Hemoglobinemia 27 0.111
23
P LKM002 Leukemia 71 0.096
24
PRT036 Peritonitis 63 0.096
25
CRB009 Cerebritis 39 0.096
26
MCR067 Microcoria, Congenital 20 0.096
27
P MLT019 Multiple Myeloma 83 0.078
28
P KDN018 Kidney Disease 66 0.078
29
BRN024 Bronchitis 64 0.078
30
P LYM026 Lymphoblastic Leukemia 62 0.078
31
P PLY018 Polycythemia 58 0.078
32
PRS047 Prostatitis 56 0.078
33
P PLY041 Polymyositis 52 0.078
34
URM002 Uremia 48 0.078
35
c CHR020 Chronic Interstitial Cystitis 41 0.078
36
NRN002 Neuronitis 41 0.078
37
AMN006 Aminoaciduria 40 0.078
38
DFF015 Diffuse Glomerulonephritis 34 0.078
39
P RNL014 Renal Cell Carcinoma 82 0.055
40
CRH001 Crohn's Disease 75 0.055
41
P LYM118 Lymphoma 69 0.055
42
P MYP004 Myopathy 67 0.055
43
VSC007 Vascular Disease 67 0.055
44
DRM006 Dermatitis 66 0.055
45
P AMY004 Amyloidosis 65 0.055
46
DFC004 Deficiency Anemia 64 0.055
47
P THR014 Thrombocytopenia 64 0.055
48
P OST002 Osteoporosis 64 0.055
49
RNL101 Renal Cell Carcinoma, Papillary 63 0.055
50
c HMP004 Hemophilia B 62 0.055
51
P HML002 Hemolytic Anemia 62 0.055
52
VSC011 Vasculitis 62 0.055
53
ISC004 Ischemia 61 0.055
54
P PSR002 Psoriasis 61 0.055
55
P CCK001 Cockayne Syndrome 61 0.055
56
P PNC044 Pancreatitis 61 0.055
57
c CNG006 Congenital Hypothyroidism 60 0.055
58
P ENC018 Encephalopathy 59 0.055
59
P NRP001 Neuropathy 59 0.055
60
P HMP007 Hemophilia 57 0.055
61
P HYP040 Hypospadias 57 0.055
62
c PRC016 Pre-Eclampsia 56 0.055
63
CHR177 Chromophobe Renal Cell Carcinoma 56 0.055
64
P PLY006 Polydactyly 56 0.055
65
P FNC043 Fanconi Anemia, Complementation Group E 55 0.055
66
NLP001 Nail-Patella Syndrome 54 0.055
67
P ECL001 Eclampsia 54 0.055
68
PRT014 Protein S Deficiency 53 0.055
69
P PLY014 Polycystic Kidney Disease 53 0.055
70
P SYP003 Syphilis 53 0.055
71
CYS010 Cystinosis 53 0.055
72
CYT008 Cytomegalovirus Infection 52 0.055
73
ALL026 Allergic Hypersensitivity Disease 52 0.055
74
P HML001 Hemolytic-Uremic Syndrome 51 0.055
75
VRC001 Varicocele 51 0.055
76
INT051 Intussusception 50 0.055
77
STM007 Stomatitis 50 0.055
78
HPT074 Hepatic Adenoma, Somatic 50 0.055
79
c SVR005 Severe Pre-Eclampsia 49 0.055
80
MCL002 Macular Corneal Dystrophy 49 0.055
81
P FNC004 Fanconi Syndrome 49 0.055
82
P RNL017 Renal Oncocytoma 47 0.055
83
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 44 0.055
84
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.055
85
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.055
86
CRS001 Crescentic Glomerulonephritis 42 0.055
87
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.055
88
c SCN006 Secondary Syphilis 41 0.055
89
MSM001 Meesmann Corneal Dystrophy 40 0.055
90
CMP009 Complement Deficiency 39 0.055
91
PCH002 Pachygyria 39 0.055
92
GLC086 Glucocorticoid-Induced Osteoporosis 38 0.055
93
HYP034 Hypertensive Encephalopathy 38 0.055
94
ISC002 Ischemic Optic Neuropathy 37 0.055
95
ASP004 Asphyxia Neonatorum 35 0.055
96
c BRN108 Branchiootic Syndrome 1 34 0.055
97
IRT001 Iritis 34 0.055
98
OCH001 Ochronosis 33 0.055
99
PRN007 Perinephritis 32 0.055
100
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.055
101
MTP028 Metaphyseal Dysplasia, Spahr Type 31 0.055
102
P IGN003 Iga Nephropathy 1 27 0.055
103
HNM002 Hinman Syndrome 25 0.055
104
EXF003 Exfoliative Dermatitis 25 0.055
105
AND005 Androgen Insensitivity Syndrome, Mild 16 0.055
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