Search results for meis2

105 hits were found for meis2

# Family MCID Name MIFTS Score
1
CLF050 Cleft Palate, Cardiac Defects, and Mental Retardation 27 42.540
2
CLF054 Cleft Palate, Cardiac Defects, and Intellectual Disability 5 17.157
3
LRN003 Learning Disability 49 14.258
4
PTR032 Peters-Plus Syndrome 63 11.938
5
P ATT013 Attention Deficit-Hyperactivity Disorder 64 11.938
6
CHR612 Chromosome 15q14 Deletion Syndrome 19 11.540
7
P AXN002 Axenfeld-Rieger Syndrome 63 10.196
8
P ORF002 Orofacial Cleft 43 9.060
9
P ANR048 Aniridia 1 64 8.442
10
CLF027 Cleft Palate, Isolated 64 7.223
11
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 5.893
12
P VNT002 Ventricular Septal Defect 58 3.990
13
P CLR023 Colorectal Cancer 100 3.590
14
P NRB001 Neuroblastoma 66 3.516
15
P PRS040 Prostate Cancer 95 3.413
16
P HYP265 Hypotonia 42 3.196
17
c ATS007 Autism Spectrum Disorder 72 3.139
18
c LKM061 Leukemia, Acute Myeloid 83 2.922
19
HRT011 Heart Septal Defect 49 2.822
20
HLX001 Helix Syndrome 48 2.822
21
GST092 Gastroesophageal Reflux 61 2.715
22
CNT061 Conotruncal Heart Malformations 66 2.539
23
MYL069 Myeloma, Multiple 77 2.539
24
c ART115 Aortic Valve Disease 1 74 2.433
25
P MYL006 Myeloid Leukemia 61 2.433
26
MCR013 Microphthalmia 60 2.433
27
CHR178 Chromosomal Triplication 34 2.320
28
CLF004 Cleft Lip/palate 57 2.198
29
CLF001 Cleft Lip 53 2.198
30
ORF053 Orofacial Clefting Syndrome 31 2.198
31
CNS004 Constipation 56 2.198
32
FRS019 Farsightedness 36 2.198
33
PRS129 Prostatic Hyperplasia, Benign 49 2.066
34
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.066
35
47X002 47,xyy 48 2.066
36
P NTR004 Neutropenia 63 2.066
37
PRS021 Prostatic Adenoma 43 2.066
38
PRS045 Prostatic Hypertrophy 53 2.066
39
EMB004 Embryonal Carcinoma 56 2.066
40
PNS015 Penoscrotal Transposition 25 2.066
41
P MYC007 Myocardial Infarction 70 1.920
42
P BLD134 Bladder Cancer 79 1.841
43
P ATS364 Autism 69 1.754
44
CHR619 Chromosome 2q35 Duplication Syndrome 64 1.754
45
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.754
46
P CRC039 Coarctation of Aorta 46 1.754
47
CLB010 Coloboma of Macula 53 1.754
48
P SCL018 Scoliosis 57 1.754
49
P SYN057 Syndromic Intellectual Disability 38 1.754
50
MNN043 Meningioma, Familial 79 1.558
51
SCR001 Secretory Meningioma 40 1.558
52
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.558
53
P LKM002 Leukemia 67 1.558
54
SPN021 Spinal Meningioma 50 1.558
55
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 1.558
56
P HPT023 Hepatocellular Carcinoma 96 1.383
57
P TTR001 Tetralogy of Fallot 69 1.301
58
DGR001 Digeorge Syndrome 62 1.301
59
P FBR017 Fibrosarcoma 56 1.237
60
P CTR002 Cataract 60 1.237
61
P PNC035 Pancreatic Cancer 86 1.170
62
P RTT002 Rett Syndrome 79 1.072
63
PLL008 Pallister-Killian Syndrome 41 1.072
64
OBS002 Obsessive-Compulsive Disorder 68 1.072
65
P OVR042 Ovarian Cancer 88 1.072
66
BRX001 Bruxism 51 1.072
67
IQS001 Iqsec2 18 1.072
68
P LNG032 Lung Cancer 98 0.875
69
PTZ001 Peutz-Jeghers Syndrome 70 0.875
70
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.875
71
c HYP518 Hypogonadotropic Hypogonadism 16 with or Without Anosmia 28 0.875
72
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.875
73
AMB001 Amebiasis 57 0.875
74
GLB002 Glioblastoma 67 0.875
75
LNG031 Lung Benign Neoplasm 51 0.875
76
c HYP532 Hypogonadotropic Hypogonadism 18 with or Without Anosmia 27 0.875
77
P LNG064 Lung Cancer Susceptibility 3 70 0.875
78
P ADN016 Adenocarcinoma 63 0.875
79
SQM006 Squamous Cell Carcinoma 60 0.875
80
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.619
81
c NPH049 Nephrotic Syndrome, Type 2 51 0.619
82
c OPT053 Optic Atrophy 1 62 0.619
83
P RST001 Restless Legs Syndrome 52 0.619
84
APR001 Apraxia 52 0.619
85
NRL016 Neural Tube Defects 81 0.619
86
P LKM062 Leukemia, Acute Lymphoblastic 69 0.619
87
c BRD017 Bardet-Biedl Syndrome 5 38 0.619
88
c HYP522 Hypogonadotropic Hypogonadism 11 with or Without Anosmia 28 0.619
89
P HNT016 Huntington Disease 73 0.619
90
c GLC092 Glaucoma, Primary Open Angle 62 0.619
91
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 0.619
92
ORL015 Oral Squamous Cell Carcinoma 43 0.619
93
P OPN001 Open-Angle Glaucoma 55 0.619
94
SPC005 Speech Disorder 45 0.619
95
CRV038 Cervical Squamous Cell Carcinoma 58 0.619
96
PRP016 Paraplegia 52 0.619
97
CRB004 Cerebral Artery Occlusion 45 0.619
98
c HRD010 Hereditary Spastic Paraplegia 66 0.619
99
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.619
100
END035 Endocrine Gland Cancer 43 0.619
101
CHL109 Childhood Apraxia of Speech 43 0.619
102
P PHC014 Phocomelia 23 0.619
103
P BRS047 Breast Cancer 98 0.551
104
P PRD006 Prader-Willi Syndrome 61 0.551
105
MYL005 Myelofibrosis 71 0.551
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