Search results for tgif1

111 hits were found for tgif1

# Family MCID Name MIFTS Score
1
P HLP001 Holoprosencephaly 69 46.707
2
c HLP029 Holoprosencephaly 4 43 44.078
3
P PRS040 Prostate Cancer 95 16.515
4
P MYP006 Myopia 56 15.429
5
SML028 Semilobar Holoprosencephaly 48 15.288
6
OTT002 Otitis Media 71 13.108
7
PTT001 Pituitary Hypoplasia 34 11.075
8
P CMR001 Camurati-Engelmann Disease 59 10.445
9
P LTT001 Lattice Corneal Dystrophy 31 10.445
10
P CRN025 Corneal Dystrophy 49 10.445
11
SLT005 Solitary Median Maxillary Central Incisor 49 8.016
12
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 44 7.903
13
LBR025 Lobar Holoprosencephaly 47 7.903
14
ALB014 Alobar Holoprosencephaly 46 7.903
15
MCR173 Microform Holoprosencephaly 44 7.903
16
SPT016 Septopreoptic Holoprosencephaly 36 7.903
17
P LYS001 Loeys-Dietz Syndrome 65 7.386
18
END059 Endocrine-Cerebroosteodysplasia 41 7.386
19
CHR211 Chromosome 18p Deletion Syndrome 38 7.386
20
CLL036 Culler-Jones Syndrome 49 7.386
21
c CRN236 Corneal Dystrophy, Lattice Type I 35 7.386
22
CRN237 Corneal Dystrophy, Avellino Type 39 7.386
23
ACT022 Acute Retinal Necrosis Syndrome 32 7.386
24
TYM002 Tympanic Membrane Disease 21 7.386
25
c BSL030 Basal Encephalocele 26 7.386
26
c CNG031 Congenital Nervous System Abnormality 24 7.386
27
EXN003 Exencephaly 30 7.386
28
c HLP023 Holoprosencephaly 1 56 5.935
29
PNC041 Pancreatic Ductal Adenocarcinoma 51 4.490
30
P CLR023 Colorectal Cancer 100 3.447
31
P PNC035 Pancreatic Cancer 86 3.414
32
P BND020 Bone Disease 59 3.294
33
ORL015 Oral Squamous Cell Carcinoma 43 2.984
34
SQM006 Squamous Cell Carcinoma 60 2.984
35
GLL048 Glial Tumor 52 2.664
36
GLM045 Glioma 63 2.664
37
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.440
38
P BRS047 Breast Cancer 98 2.415
39
c LKM061 Leukemia, Acute Myeloid 83 2.317
40
P MYL006 Myeloid Leukemia 61 2.317
41
ORL011 Oral Cancer 60 2.317
42
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.273
43
BNR002 Bone Resorption Disease 47 2.182
44
THY029 Thyroid Carcinoma 51 2.182
45
c HLP028 Holoprosencephaly 5 47 2.033
46
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 35 1.993
47
BCT022 Bacterial Infectious Disease 56 1.664
48
P SZR006 Seizure Disorder 70 1.409
49
c MCR130 Microvascular Complications of Diabetes 6 41 1.409
50
c MCR120 Microvascular Complications of Diabetes 7 47 1.409
51
c MCR113 Microvascular Complications of Diabetes 3 52 1.409
52
c MCR133 Microvascular Complications of Diabetes 4 41 1.409
53
SPN186 Spinal Cord Injury 61 1.092
54
HLC007 Helicobacter Pylori Infection 67 1.092
55
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.092
56
P LNG064 Lung Cancer Susceptibility 3 70 1.092
57
BRN012 Bronchiolitis Obliterans 56 1.092
58
P ADN016 Adenocarcinoma 63 1.092
59
P END044 Endometriosis 62 1.092
60
P INF032 Infertility 57 1.092
61
BRN002 Bronchiolitis 57 1.092
62
FRY006 Fryns Microphthalmia Syndrome 52 0.891
63
c BRN108 Branchiootic Syndrome 1 62 0.891
64
RNL077 Renal Fibrosis 46 0.891
65
P HYP730 Hypogonadotropic Hypogonadism 53 0.891
66
P ISL020 Isolated Microphthalmia 23 0.891
67
URT010 Ureteral Obstruction 45 0.891
68
END086 End Stage Renal Disease 52 0.891
69
MCR013 Microphthalmia 60 0.891
70
HYP080 Hypogonadism 50 0.891
71
LYM133 Lymphoma, Hodgkin, Classic 74 0.630
72
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.630
73
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.630
74
c HLP024 Holoprosencephaly 2 49 0.630
75
P PHC003 Pheochromocytoma 69 0.630
76
CLF027 Cleft Palate, Isolated 64 0.630
77
P FML011 Familial Adenomatous Polyposis 71 0.630
78
MLG157 Malignant Pheochromocytoma 36 0.630
79
P LYM118 Lymphoma 67 0.630
80
c FNC043 Fanconi Anemia, Complementation Group E 62 0.630
81
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.630
82
P FNC044 Fanconi Anemia, Complementation Group C 56 0.630
83
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.630
84
c HLP022 Holoprosencephaly 8 22 0.630
85
TTR014 Tetrasomy 18p 31 0.630
86
CNT061 Conotruncal Heart Malformations 66 0.630
87
SPT006 Septooptic Dysplasia 62 0.630
88
HYP748 Hypertelorism 46 0.630
89
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.630
90
c HLP026 Holoprosencephaly 3 48 0.630
91
ADR040 Adrenal Gland Pheochromocytoma 46 0.630
92
P KLL001 Kallmann Syndrome 65 0.630
93
SPC005 Speech Disorder 45 0.630
94
47X002 47,xyy 48 0.630
95
CNG562 Congenital Hypogonadotropic Hypogonadism 33 0.630
96
P LVR013 Liver Disease 69 0.630
97
P EPL164 Epilepsy 68 0.630
98
P TRN020 Turner Syndrome 67 0.630
99
P PLM036 Pulmonary Fibrosis 66 0.630
100
P ART022 Arthritis 71 0.630
101
LNG099 Lung Disease 62 0.630
102
P END046 Endometritis 46 0.630
103
P TMP001 Temporal Lobe Epilepsy 49 0.630
104
P GND004 Gonadal Dysgenesis 47 0.630
105
P DRR001 Diarrhea 55 0.630
106
18P001 18p Deletion Syndrome 13 0.630
107
c JVN010 Juvenile Rheumatoid Arthritis 66 0.630
108
PTT041 Pituitary Stalk Interruption Syndrome 54 0.630
109
HMP009 Haemophilus Influenzae 41 0.630
110
PNS014 Penis Agenesis 36 0.630
111
P LKM062 Leukemia, Acute Lymphoblastic 69 0.551
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