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Search results for nog

124 hits were found for nog

# Family MCID Name MIFTS Score
1
TRS002 Tarsal-Carpal Coalition Syndrome 42 12.637
2
c MLT059 Multiple Synostoses Syndrome 1 33 4.740
3
c SYM022 Symphalangism, Proximal, 1a 33 4.740
4
c BRC052 Brachydactyly, Type B2 41 4.650
5
P MLT072 Multiple Synostoses Syndrome 39 4.189
6
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 3.978
7
P PRX021 Proximal Symphalangism 46 3.723
8
ANK001 Ankylosis 51 3.581
9
P BRC006 Brachydactyly 53 3.486
10
P PRS040 Prostate Cancer 97 3.289
11
SYN005 Synostosis 45 3.028
12
P OTS001 Otosclerosis 49 2.929
13
NRL016 Neural Tube Defects 82 2.878
14
P OST002 Osteoporosis 74 2.878
15
FBR011 Fibrodysplasia Ossificans Progressiva 67 2.878
16
ESP020 Esophageal Atresia 62 2.878
17
P CRN037 Craniosynostosis 68 2.848
18
c BRC051 Brachydactyly, Type B1 51 2.419
19
P HLP001 Holoprosencephaly 67 2.361
20
CLF027 Cleft Palate, Isolated 64 2.361
21
PFF001 Pfeiffer Syndrome 79 2.325
22
OSS012 Osseous Heteroplasia, Progressive 61 2.325
23
P BND020 Bone Disease 59 2.325
24
P SCL048 Sclerosteosis 55 2.325
25
CHR619 Chromosome 2q35 Duplication Syndrome 62 1.758
26
FRS019 Farsightedness 38 1.727
27
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 1.691
28
P RTN008 Retinitis Pigmentosa 79 1.644
29
P JVN014 Juvenile Polyposis Syndrome 68 1.644
30
HYL004 Hyaline Fibromatosis Syndrome 67 1.644
31
c BRC078 Brachydactyly, Type A1 56 1.644
32
c BRC079 Brachydactyly, Type A2 51 1.644
33
CMB003 Combined T Cell and B Cell Immunodeficiency 49 1.644
34
DPN005 Du Pan Syndrome 48 1.644
35
P ORF002 Orofacial Cleft 44 1.644
36
DYS018 Dysostosis 44 1.644
37
SYN031 Synovial Chondromatosis 42 1.644
38
ABR009 Abruzzo-Erickson Syndrome 41 1.644
39
c BRC080 Brachydactyly, Type A1, B 38 1.644
40
SYN086 Synostoses, Tarsal, Carpal, and Digital 35 1.644
41
HMR015 Humeroradial Synostosis 33 1.644
42
P BND014 Bone Development Disease 33 1.644
43
c BRC075 Brachydactyly, Type A1, C 32 1.644
44
SGR001 Sugarman Brachydactyly 30 1.644
45
GRM001 Germ Cell and Embryonal Cancer 29 1.644
46
SVR004 Severe Combined Immunodeficiency 73 0.400
47
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.219
48
P GRF003 Graft-Versus-Host Disease 72 0.139
49
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.127
50
P CLR023 Colorectal Cancer 99 0.113
51
c BRN108 Branchiootic Syndrome 1 62 0.113
52
P CTR002 Cataract 60 0.098
53
MYL069 Myeloma, Multiple 85 0.080
54
P PNC035 Pancreatic Cancer 84 0.080
55
P MLN008 Melanoma 69 0.080
56
OST017 Osteomyelitis 64 0.080
57
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.080
58
P SNS001 Sensorineural Hearing Loss 60 0.080
59
P MYS005 Myositis 56 0.080
60
c ACT134 Acute Liver Failure 56 0.080
61
P HYP083 Hypopituitarism 53 0.080
62
P OVR082 Overgrowth Syndrome 50 0.080
63
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.080
64
c LKM061 Leukemia, Acute Myeloid 84 0.057
65
IMM167 Immune Deficiency Disease 78 0.057
66
c LKM063 Leukemia, Chronic Myeloid 72 0.057
67
AGM019 Agammaglobulinemia, X-Linked 71 0.057
68
c EXD008 Exudative Vitreoretinopathy 1 71 0.057
69
MYL005 Myelofibrosis 70 0.057
70
P OST001 Osteopetrosis 70 0.057
71
PLY001 Polycythemia Vera 69 0.057
72
P LYM118 Lymphoma 68 0.057
73
P ESS003 Essential Thrombocythemia 68 0.057
74
BRK010 Burkitt Lymphoma 67 0.057
75
P SKN015 Skin Carcinoma 66 0.057
76
P AGM001 Agammaglobulinemia 65 0.057
77
P HRP006 Herpes Simplex 65 0.057
78
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.057
79
P RHB003 Rhabdomyosarcoma 63 0.057
80
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.057
81
ATM095 Autoimmune Disease 62 0.057
82
RTN017 Retinal Detachment 61 0.057
83
P MYL006 Myeloid Leukemia 60 0.057
84
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.057
85
c HPT016 Hepatitis B 59 0.057
86
ADN018 Adenoma 59 0.057
87
P PLY006 Polydactyly 59 0.057
88
P PLY018 Polycythemia 56 0.057
89
P ADL017 Adult T-Cell Leukemia 56 0.057
90
SFT003 Soft Tissue Sarcoma 56 0.057
91
P STR020 Strabismus 55 0.057
92
P ALP008 Alopecia 54 0.057
93
CLF001 Cleft Lip 53 0.057
94
P PTS002 Ptosis 53 0.057
95
P RTN018 Retinal Disease 53 0.057
96
P TRT010 Teratoma 52 0.057
97
P LCT001 Lactic Acidosis 51 0.057
98
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.057
99
BLR001 Biliary Atresia 50 0.057
100
TRP002 Tropical Spastic Paraparesis 50 0.057
101
AMB002 Amblyopia 49 0.057
102
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.057
103
SPL018 Splenomegaly 48 0.057
104
MLK006 Milk Allergy 48 0.057
105
CLF056 Cleft Lip with or Without Cleft Palate 47 0.057
106
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.057
107
P VTR007 Vitreoretinopathy 46 0.057
108
MCR173 Microform Holoprosencephaly 44 0.057
109
HPT067 Hepatocellular Adenoma 44 0.057
110
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.057
111
MCH006 Mechanical Strabismus 42 0.057
112
CWM001 Cow Milk Allergy 40 0.057
113
SPP007 Suppression Amblyopia 39 0.057
114
MYL057 Myelopathy, Htlv-1-Associated 39 0.057
115
SPS019 Spastic Paraparesis 38 0.057
116
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.057
117
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 37 0.057
118
c CHR020 Chronic Interstitial Cystitis 37 0.057
119
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.057
120
c LKM005 Leukemia, T-Cell, Chronic 34 0.057
121
c SYM019 Symphalangism, Proximal, 1b 24 0.057
122
TRS030 Tarsal Coalition 22 0.057
123
P SPN237 Spina Bifida Aperta 20 0.057
124
THS001 Thai Symphalangism Syndrome 12 0.057
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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