Search results for OSM

65 hits were found for OSM

# Family MCID Name MIFTS Score
1
c OTS013 Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive 57 8.860
2
P OTS014 Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant 52 6.227
3
P ART022 Arthritis 69 4.304
4
P RHM011 Rheumatoid Arthritis 80 3.764
5
KPS004 Kaposi Sarcoma 75 3.728
6
P PSR002 Psoriasis 62 3.728
7
PLS011 Plasmacytoma 56 3.728
8
c BRS049 Breast Carcinoma in Situ 51 3.087
9
c AMY091 Amyotrophic Lateral Sclerosis 1 89 3.043
10
c ART144 Arthrogryposis, Distal, Type 1a 61 3.043
11
NNT012 Neonatal Jaundice 53 3.043
12
CHR563 Chronic Eosinophilic Leukemia 48 3.043
13
OBS082 Obstructive Nephropathy 42 3.043
14
CRB036 Cerebral Meningioma 34 3.043
15
OST016 Osteochondrosis 53 2.152
16
SDK001 Sodoku Disease 40 2.152
17
P LKM002 Leukemia 68 0.204
18
P MLN008 Melanoma 69 0.180
19
SKN019 Skin Melanoma 68 0.136
20
c BRN108 Branchiootic Syndrome 1 62 0.136
21
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.136
22
P STC001 Stickler Syndrome 56 0.136
23
P MLT020 Multiple Sclerosis 72 0.118
24
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.118
25
LNG099 Lung Disease 60 0.118
26
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.118
27
P SNS001 Sensorineural Hearing Loss 60 0.118
28
LYM027 Lymphopenia 58 0.118
29
THR004 Thrombocytosis 51 0.118
30
MYL069 Myeloma, Multiple 85 0.096
31
OST012 Osteoarthritis 78 0.096
32
MRS002 Marshall Syndrome 58 0.096
33
P INF037 Inflammatory Bowel Disease 54 0.096
34
P INS002 in Situ Carcinoma 53 0.096
35
HLX001 Helix Syndrome 47 0.096
36
c DFN137 Deafness, Autosomal Dominant 13 33 0.096
37
P BRS047 Breast Cancer 97 0.068
38
c SYS001 Systemic Lupus Erythematosus 86 0.068
39
P GLM040 Glioma Susceptibility 1 81 0.068
40
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.068
41
AST005 Asthma 76 0.068
42
GLB015 Glioblastoma Multiforme 75 0.068
43
P NRB001 Neuroblastoma 72 0.068
44
P MYC007 Myocardial Infarction 70 0.068
45
P LKM062 Leukemia, Acute Lymphoblastic 69 0.068
46
CLF027 Cleft Palate, Isolated 64 0.068
47
P GLM045 Glioma 63 0.068
48
TXC005 Toxic Shock Syndrome 62 0.068
49
LVR012 Liver Cirrhosis 62 0.068
50
P LPS004 Lupus Erythematosus 61 0.068
51
DCT002 Ductal Carcinoma in Situ 59 0.068
52
ISC004 Ischemia 58 0.068
53
VGT001 Vogt-Koyanagi-Harada Disease 55 0.068
54
P MYP006 Myopia 55 0.068
55
KNS001 Kniest Dysplasia 53 0.068
56
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.068
57
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.068
58
HYP748 Hypertelorism 50 0.068
59
ATS010 Autosomal Recessive Disease 48 0.068
60
CHR074 Choriocarcinoma 47 0.068
61
GLL048 Glial Tumor 45 0.068
62
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.068
63
DWR001 Dwarfism 44 0.068
64
PPL052 Papillomatosis, Confluent and Reticulated 33 0.068
65
MGP001 Megaepiphyseal Dwarfism 15 0.068
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