Search results for en2

120 hits were found for en2

# Family MCID Name MIFTS Score
1
P ATS364 Autism 72 20.134
2
c ATS007 Autism Spectrum Disorder 72 15.866
3
P PRK057 Parkinson Disease, Late-Onset 79 11.781
4
c ATS172 Autism 10 16 11.454
5
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 8.330
6
c CHR697 Charcot-Marie-Tooth Disease X-Linked Recessive 4 33 8.330
7
CRR002 Currarino Syndrome 49 8.330
8
DSS008 Disease of Mental Health 74 8.330
9
P PRS040 Prostate Cancer 95 3.035
10
P OVR042 Ovarian Cancer 88 1.769
11
P CLR023 Colorectal Cancer 100 1.648
12
P BLD134 Bladder Cancer 79 1.647
13
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.522
14
GLM045 Glioma 62 1.407
15
GLL048 Glial Tumor 52 1.407
16
P CRB045 Cerebellar Hypoplasia 40 1.267
17
BRN028 Brain Cancer 73 1.243
18
OVR094 Ovarian Epithelial Cancer 39 1.219
19
CRB004 Cerebral Artery Occlusion 46 1.103
20
GLB002 Glioblastoma 67 1.103
21
P HYP086 Hypothyroidism 69 1.027
22
SDD001 Sudden Infant Death Syndrome 60 1.027
23
SMT008 Smith-Magenis Syndrome 53 0.978
24
c SPR009 Sporadic Breast Cancer 42 0.978
25
P JBR020 Joubert Syndrome 1 74 0.916
26
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.916
27
c SPN101 Spinocerebellar Ataxia 29 58 0.916
28
P HYP265 Hypotonia 42 0.916
29
PTH003 Pathologic Nystagmus 52 0.916
30
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.909
31
CLR030 Clear Cell Renal Cell Carcinoma 54 0.896
32
P BRS047 Breast Cancer 97 0.779
33
P PNC035 Pancreatic Cancer 86 0.702
34
PRS129 Prostatic Hyperplasia, Benign 48 0.587
35
c LSS005 Lissencephaly 1 57 0.587
36
PRS021 Prostatic Adenoma 43 0.587
37
PRS045 Prostatic Hypertrophy 52 0.587
38
CRB037 Cerebral Palsy 67 0.587
39
P SZR006 Seizure Disorder 69 0.587
40
SQM006 Squamous Cell Carcinoma 59 0.567
41
CKT002 Cakut 48 0.551
42
c SML038 Small Cell Cancer of the Lung 69 0.502
43
ALL029 Allergic Disease 61 0.454
44
BLD131 Bladder Urothelial Carcinoma 59 0.371
45
LRN003 Learning Disability 49 0.371
46
FTL006 Fetal Alcohol Spectrum Disorder 43 0.303
47
SPC010 Speech and Communication Disorders 48 0.303
48
P PLY006 Polydactyly 58 0.303
49
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.303
50
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 0.262
51
P MLN008 Melanoma 75 0.262
52
P HLP001 Holoprosencephaly 69 0.262
53
SKN019 Skin Melanoma 70 0.262
54
EXN003 Exencephaly 30 0.262
55
P MDL005 Medulloblastoma 75 0.214
56
P FLL037 Follicular Lymphoma 73 0.214
57
P HNT016 Huntington Disease 73 0.214
58
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.214
59
P EPL164 Epilepsy 70 0.214
60
P MCR010 Microcephaly 59 0.214
61
P OVR082 Overgrowth Syndrome 42 0.214
62
ACR020 Acropectorovertebral Dysplasia 23 0.151
63
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.151
64
RHB024 Rhabdomyosarcoma 2 65 0.151
65
P PHS005 Peho Syndrome 44 0.151
66
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.151
67
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.151
68
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.151
69
ONC007 Oncocytoma 49 0.151
70
ACR019 Acropectoral Syndrome 20 0.151
71
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.151
72
HLX001 Helix Syndrome 47 0.151
73
MCR013 Microphthalmia 60 0.151
74
IMM167 Immune Deficiency Disease 77 0.151
75
UTR056 Uterine Corpus Endometrial Carcinoma 27 0.151
76
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.151
77
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.151
78
END057 Endometrial Cancer 71 0.151
79
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.151
80
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.151
81
c HLP026 Holoprosencephaly 3 48 0.151
82
KPS004 Kaposi Sarcoma 76 0.151
83
CLF027 Cleft Palate, Isolated 64 0.151
84
NRL016 Neural Tube Defects 81 0.151
85
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.151
86
c HYP511 Hypogonadotropic Hypogonadism 15 with or Without Anosmia 28 0.151
87
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.151
88
c HYP538 Hypogonadotropic Hypogonadism 17 with or Without Anosmia 25 0.151
89
c HYP546 Hypogonadotropic Hypogonadism 20 with or Without Anosmia 23 0.151
90
P FRG001 Fragile X Syndrome 70 0.151
91
c HYP523 Hypogonadotropic Hypogonadism 14 with or Without Anosmia 29 0.151
92
SRC014 Sarcoma 64 0.151
93
P GLM040 Glioma Susceptibility 1 70 0.151
94
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.151
95
P PRV002 Periventricular Nodular Heterotopia 52 0.151
96
P SCK004 Seckel Syndrome 58 0.151
97
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.151
98
MLG169 Malignant Astrocytoma 57 0.151
99
P LNG028 Long Qt Syndrome 63 0.151
100
P RNL017 Renal Oncocytoma 54 0.151
101
P PLC011 Pilocytic Astrocytoma 55 0.151
102
P LKM002 Leukemia 66 0.151
103
P RHB003 Rhabdomyosarcoma 66 0.151
104
c LKM061 Leukemia, Acute Myeloid 83 0.151
105
c ORF050 Orofacial Cleft 2 19 0.151
106
c NPH032 Nephronophthisis 4 45 0.151
107
HRL003 Hurler Syndrome 66 0.151
108
P NSP012 Nasopharyngeal Carcinoma 60 0.151
109
c RNG014 Ring Chromosome 19 17 0.151
110
SPN035 Spindle Cell Sarcoma 51 0.151
111
P NRB001 Neuroblastoma 66 0.151
112
CLF001 Cleft Lip 54 0.151
113
P RBL001 Rubella 58 0.151
114
CHR178 Chromosomal Triplication 34 0.151
115
CNG124 Congenital Rubella 43 0.151
116
FTL029 Fetal Thalidomide Syndrome 26 0.151
117
DWR001 Dwarfism 45 0.151
118
CLF056 Cleft Lip with or Without Cleft Palate 43 0.151
119
HMM005 Hemimelia 33 0.151
120
P RNG032 Ring Chromosome 39 0.151
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