Search results for nog

60 hits were found for nog

# Family MCID Name MIFTS Score
1
TRS002 Tarsal-Carpal Coalition Syndrome 36 13.666
2
P PRX021 Proximal Symphalangism 49 5.665
3
c MLT059 Multiple Synostoses Syndrome 1 30 5.406
4
c BRC052 Brachydactyly, Type B2 44 5.356
5
c SYM022 Symphalangism, Proximal, 1a 28 5.252
6
P MLT072 Multiple Synostoses Syndrome 45 4.705
7
STP011 Stapes Ankylosis with Broad Thumbs and Toes 40 4.685
8
ANK001 Ankylosis 56 4.105
9
P BRC006 Brachydactyly 50 3.955
10
SYN005 Synostosis 51 3.600
11
FBR011 Fibrodysplasia Ossificans Progressiva 65 3.570
12
ESP020 Esophageal Atresia 53 3.570
13
P OTS001 Otosclerosis 53 3.570
14
P CRN037 Craniosynostosis 66 3.538
15
NRL016 Neural Tube Defects 79 3.101
16
P OST002 Osteoporosis 74 3.101
17
c BRC051 Brachydactyly, Type B1 54 3.101
18
TRC040 Tracheoesophageal Fistula 48 3.101
19
P SCL048 Sclerosteosis 48 3.064
20
P HLP001 Holoprosencephaly 65 2.545
21
CHR619 Chromosome 2q35 Duplication Syndrome 60 2.545
22
SPN060 Spondylocarpotarsal Synostosis Syndrome 59 2.501
23
OSS012 Osseous Heteroplasia, Progressive 58 2.501
24
SYN031 Synovial Chondromatosis 48 2.501
25
c BRC079 Brachydactyly, Type A2 46 2.501
26
c BRC081 Brachydactyly, Type C 45 2.501
27
FBL002 Fibular Hypoplasia and Complex Brachydactyly 42 2.501
28
SYN086 Synostoses, Tarsal, Carpal, and Digital 37 2.501
29
FRS019 Farsightedness 36 2.501
30
ABR009 Abruzzo-Erickson Syndrome 33 2.501
31
HMR015 Humeroradial Synostosis 28 2.501
32
CHM005 Chemical Colitis 23 2.501
33
BND014 Bone Development Disease 30 1.769
34
MLN008 Melanoma 63 0.120
35
P PNC035 Pancreatic Cancer 82 0.098
36
c ACT134 Acute Liver Failure 53 0.098
37
c INF145 Infantile Liver Failure Syndrome 1 47 0.098
38
P BRS047 Breast Cancer 100 0.069
39
MYL069 Myeloma, Multiple 85 0.069
40
c LKM061 Leukemia, Acute Myeloid 81 0.069
41
P LKM002 Leukemia 72 0.069
42
P GRF003 Graft-Versus-Host Disease 71 0.069
43
MYL005 Myelofibrosis 69 0.069
44
c PRM196 Premature Ovarian Failure 1 68 0.069
45
P MYL006 Myeloid Leukemia 67 0.069
46
CLF027 Cleft Palate, Isolated 64 0.069
47
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 62 0.069
48
P CTR002 Cataract 59 0.069
49
P PLY006 Polydactyly 57 0.069
50
P RHB003 Rhabdomyosarcoma 57 0.069
51
CLF001 Cleft Lip 56 0.069
52
END081 Endosteal Hyperostosis, Autosomal Dominant 56 0.069
53
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 55 0.069
54
BLR001 Biliary Atresia 55 0.069
55
c HMN021 Human T-Cell Leukemia Virus Type 1 53 0.069
56
P PLY147 Polydactyly, Postaxial, Type A1 48 0.069
57
NRL018 Neural Tube Defects, Folate-Sensitive 47 0.069
58
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 46 0.069
59
c CHR020 Chronic Interstitial Cystitis 39 0.069
60
HPT070 Hepatosplenic T-Cell Lymphoma 35 0.069
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