Search results for id2

116 hits were found for id2

# Family MCID Name MIFTS Score
1
EWN003 Ewing Sarcoma 68 4.085
2
P NRB001 Neuroblastoma 71 3.598
3
P RTT002 Rett Syndrome 80 3.326
4
HYD002 Hydronephrosis 59 3.326
5
P ATT013 Attention Deficit-Hyperactivity Disorder 64 3.291
6
P DMN001 Diamond-Blackfan Anemia 69 2.327
7
LJH001 Lujo Hemorrhagic Fever 31 2.327
8
HLX001 Helix Syndrome 47 0.551
9
P RTN024 Retinoblastoma 72 0.230
10
c FML008 Familial Retinoblastoma 53 0.230
11
c LKM061 Leukemia, Acute Myeloid 83 0.121
12
GLB015 Glioblastoma Multiforme 75 0.109
13
P LYM118 Lymphoma 68 0.109
14
P LKM002 Leukemia 66 0.109
15
P GLM045 Glioma 63 0.109
16
P HPT023 Hepatocellular Carcinoma 100 0.094
17
LYM133 Lymphoma, Hodgkin, Classic 69 0.094
18
BRK010 Burkitt Lymphoma 67 0.094
19
MSC007 Muscle Hypertrophy 63 0.094
20
ATM095 Autoimmune Disease 61 0.094
21
P MYL006 Myeloid Leukemia 60 0.094
22
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.094
23
P PLY014 Polycystic Kidney Disease 59 0.094
24
GLL048 Glial Tumor 45 0.094
25
P CLR023 Colorectal Cancer 98 0.077
26
P PNC035 Pancreatic Cancer 84 0.077
27
MLN008 Melanoma 69 0.077
28
P LKM062 Leukemia, Acute Lymphoblastic 68 0.077
29
OST159 Osteogenic Sarcoma 66 0.077
30
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.077
31
c PRC016 Pre-Eclampsia 63 0.077
32
ACT119 Acute Promyelocytic Leukemia 63 0.077
33
P END044 Endometriosis 62 0.077
34
ISC004 Ischemia 60 0.077
35
SPN186 Spinal Cord Injury 60 0.077
36
P VNT002 Ventricular Septal Defect 60 0.077
37
SQM006 Squamous Cell Carcinoma 60 0.077
38
c ACT073 Acute Leukemia 58 0.077
39
P BCL017 B-Cell Lymphoma 58 0.077
40
HYP266 Hypoxia 56 0.077
41
DBL002 Double Outlet Right Ventricle 56 0.077
42
P LYM031 Lymphocytic Leukemia 55 0.077
43
P MNC007 Monocytic Leukemia 54 0.077
44
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.077
45
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.077
46
CRB004 Cerebral Artery Occlusion 44 0.077
47
ORL015 Oral Squamous Cell Carcinoma 43 0.077
48
ALL014 Allergic Encephalomyelitis 39 0.077
49
P LNG032 Lung Cancer 97 0.054
50
P OVR042 Ovarian Cancer 89 0.054
51
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.054
53
P GST053 Gastric Cancer 83 0.054
54
c FNC027 Fanconi Anemia, Complementation Group a 81 0.054
55
INS024 Insulin-Like Growth Factor I 79 0.054
56
P BLD134 Bladder Cancer 78 0.054
57
P LNG064 Lung Cancer Susceptibility 3 77 0.054
58
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.054
59
DFC004 Deficiency Anemia 75 0.054
60
SVR004 Severe Combined Immunodeficiency 73 0.054
61
P FML011 Familial Adenomatous Polyposis 72 0.054
62
P GRF003 Graft-Versus-Host Disease 71 0.054
63
c HPT073 Hepatitis C Virus 70 0.054
64
P PLM037 Pulmonary Hypertension 68 0.054
65
P INF038 Influenza 68 0.054
66
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.054
67
P MSC005 Muscular Dystrophy 66 0.054
68
SRC014 Sarcoma 65 0.054
69
c SML038 Small Cell Cancer of the Lung 65 0.054
70
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.054
71
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.054
72
ALL026 Allergic Hypersensitivity Disease 64 0.054
73
CLN015 Colon Adenocarcinoma 63 0.054
74
P ANP001 Anaplastic Large Cell Lymphoma 61 0.054
75
P SLV026 Salivary Gland Carcinoma 60 0.054
76
ORL011 Oral Cancer 60 0.054
77
DCT002 Ductal Carcinoma in Situ 59 0.054
78
P MLN069 Melanoma, Uveal 58 0.054
79
P MCR010 Microcephaly 58 0.054
80
PLC005 Placental Insufficiency 57 0.054
81
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.054
82
ERY051 Erythroleukemia, Familial 56 0.054
83
P FBR017 Fibrosarcoma 56 0.054
84
P MLN007 Male Infertility 56 0.054
85
OCL009 Ocular Cancer 55 0.054
86
PPL022 Papilloma 54 0.054
87
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.054
88
c ACT020 Acute T Cell Leukemia 53 0.054
89
P LTR001 Lateral Sclerosis 53 0.054
90
DMY004 Demyelinating Disease 52 0.054
91
P INS002 in Situ Carcinoma 52 0.054
92
P MSC003 Muscular Atrophy 52 0.054
93
c ACT135 Acute Graft Versus Host Disease 51 0.054
94
P ECL001 Eclampsia 51 0.054
95
SPN035 Spindle Cell Sarcoma 51 0.054
96
c PNC106 Pancreatic Agenesis 1 50 0.054
97
c FNC029 Fanconi Anemia, Complementation Group I 50 0.054
98
P OVR082 Overgrowth Syndrome 50 0.054
99
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 49 0.054
100
LFT001 Left Bundle Branch Hemiblock 49 0.054
101
BNR002 Bone Resorption Disease 48 0.054
102
GNG008 Ganglioneuroblastoma 47 0.054
103
P TCL004 T-Cell Leukemia 47 0.054
104
PNC034 Pancreas Disease 46 0.054
105
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.054
106
LYM009 Lymphocytic Choriomeningitis 46 0.054
107
P HMN032 Human Herpesvirus 8 46 0.054
108
TRT001 Teratocarcinoma 46 0.054
109
c MLG068 Malignant Glioma 45 0.054
110
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 45 0.054
111
PTT037 Pituitary Tumors 44 0.054
112
SQM002 Squamous Cell Papilloma 42 0.054
113
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.054
114
GRN022 Granulosa Cell Tumor of the Ovary 33 0.054
115
CND006 Candida Glabrata 32 0.054
116
INT029 Interleukin-7 Receptor Alpha Deficiency 22 0.054
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