Search results for "nephrosis, congenital, with or without ocular abnormalities"

The MalaCard for "nephrosis, congenital, with or without ocular abnormalities" has been retired.
Searching MalaCards for entries containing "nephrosis, congenital, with or without ocular abnormalities"

54 hits were found for 'nephrosis, congenital, with or without ocular abnormalities'

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 70 0.390
2
P HPT021 Hepatitis 74 0.373
3
P LYM118 Lymphoma 68 0.359
4
LPD004 Lipoid Nephrosis 49 0.325
5
END072 Endotheliitis 41 0.275
6
CRB009 Cerebritis 36 0.247
7
P HYP086 Hypothyroidism 63 0.214
8
P LYM026 Lymphoblastic Leukemia 60 0.209
9
P MYP004 Myopathy 67 0.206
10
NRN002 Neuronitis 40 0.204
11
P NRP001 Neuropathy 57 0.201
12
P KDN018 Kidney Disease 64 0.201
13
P MYL007 Myeloma 52 0.196
14
P ENC018 Encephalopathy 59 0.195
15
PRS047 Prostatitis 56 0.193
16
c MLT019 Multiple Myeloma 77 0.192
17
P NPH012 Nephrotic Syndrome 55 0.184
18
P GLM007 Glomerulonephritis 56 0.178
19
VSC007 Vascular Disease 51 0.165
20
ISC004 Ischemia 56 0.164
21
PRT036 Peritonitis 65 0.157
22
P SYP003 Syphilis 51 0.148
23
P THR014 Thrombocytopenia 63 0.142
24
CYT008 Cytomegalovirus Infection 51 0.139
25
DRM006 Dermatitis 58 0.136
26
GLM011 Glomerulosclerosis 41 0.134
27
VSC011 Vasculitis 62 0.131
28
P AMY004 Amyloidosis 63 0.128
29
P PLY018 Polycythemia 58 0.122
30
P OST002 Osteoporosis 63 0.122
31
GNG013 Gingivitis 61 0.121
32
P PSR002 Psoriasis 63 0.118
33
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.112
34
CRH001 Crohn's Disease 76 0.112
35
P FCL005 Focal Segmental Glomerulosclerosis 59 0.109
36
P PLY006 Polydactyly 56 0.105
37
BRN024 Bronchitis 67 0.097
38
INT067 Interstitial Nephritis 48 0.096
39
ACN011 Acne 63 0.096
40
c BRN108 Branchiootic Syndrome 1 36 0.095
41
P HYP040 Hypospadias 58 0.091
42
BCT002 Bacterial Vaginosis 53 0.090
43
PRS055 Pierson Syndrome 40 0.082
44
PRT014 Protein S Deficiency 54 0.079
45
P FNC004 Fanconi Syndrome 54 0.073
46
P CCK001 Cockayne Syndrome 58 0.072
47
ISC002 Ischemic Optic Neuropathy 45 0.071
48
LMB050 Limbal Stem Cell Deficiency 44 0.071
49
AMN006 Aminoaciduria 39 0.070
50
P HML001 Hemolytic-Uremic Syndrome 50 0.070
51
PCH002 Pachygyria 39 0.061
52
NLP001 Nail-Patella Syndrome 54 0.060
53
c SCN006 Secondary Syphilis 41 0.058
54
PRR008 Periarteritis Nodosa 28 0.057