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"

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

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 70 0.382
2
P HPT021 Hepatitis 70 0.373
3
P LYM118 Lymphoma 70 0.361
4
LPD004 Lipoid Nephrosis 48 0.323
5
END072 Endotheliitis 42 0.274
6
CRB009 Cerebritis 38 0.246
7
VSC007 Vascular Disease 67 0.237
8
P ART022 Arthritis 75 0.234
9
P HYP086 Hypothyroidism 65 0.209
10
P LYM026 Lymphoblastic Leukemia 60 0.204
11
P NRP001 Neuropathy 60 0.201
12
P MYP004 Myopathy 67 0.201
13
NRN002 Neuronitis 42 0.195
14
PRS047 Prostatitis 56 0.188
15
P MLT019 Multiple Myeloma 80 0.188
16
P ENC018 Encephalopathy 59 0.182
17
P GLM007 Glomerulonephritis 56 0.172
18
ISC004 Ischemia 59 0.164
19
ALL026 Allergic Hypersensitivity Disease 53 0.163
20
PRT036 Peritonitis 62 0.152
21
P SYP003 Syphilis 53 0.149
22
P THR014 Thrombocytopenia 64 0.141
23
CYT008 Cytomegalovirus Infection 51 0.140
24
DRM006 Dermatitis 61 0.136
25
VSC011 Vasculitis 62 0.130
26
GLM011 Glomerulosclerosis 44 0.128
27
P AMY004 Amyloidosis 64 0.128
28
P OST002 Osteoporosis 64 0.122
29
P PSR002 Psoriasis 63 0.118
30
P PLY018 Polycythemia 57 0.116
31
CRH001 Crohn's Disease 76 0.113
32
GNG013 Gingivitis 60 0.109
33
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.108
34
HPT074 Hepatic Adenoma, Somatic 51 0.107
35
P FCL005 Focal Segmental Glomerulosclerosis 59 0.103
36
HNM002 Hinman Syndrome 25 0.103
37
P PLY006 Polydactyly 55 0.097
38
c NPH055 Nephrotic Syndrome, Type 1 59 0.094
39
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.093
40
BRN024 Bronchitis 63 0.090
41
P HYP040 Hypospadias 57 0.090
42
ACN011 Acne 63 0.087
43
PRS055 Pierson Syndrome 40 0.078
44
STM007 Stomatitis 50 0.078
45
BCT002 Bacterial Vaginosis 51 0.076
46
c BRN108 Branchiootic Syndrome 1 36 0.075
47
CHR005 Chorioamnionitis 48 0.073
48
P HML001 Hemolytic-Uremic Syndrome 50 0.072
49
P CCK001 Cockayne Syndrome 59 0.071
50
P LCH002 Lichen Planus 53 0.069
51
ISC002 Ischemic Optic Neuropathy 46 0.069
52
AMN006 Aminoaciduria 42 0.062
53
LMB050 Limbal Stem Cell Deficiency 45 0.061
54
NLP001 Nail-Patella Syndrome 54 0.057
55
c SCN006 Secondary Syphilis 41 0.056
56
PCH002 Pachygyria 36 0.055
57
P DNR003 Duane Retraction Syndrome 1 39 0.049