Search results for FOXF1

98 hits were found for FOXF1

# Family MCID Name MIFTS Score
1
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 6.140
2
PRS030 Persistent Fetal Circulation Syndrome 52 4.889
3
P PLM037 Pulmonary Hypertension 67 3.384
4
PYL006 Pyloric Stenosis 48 3.207
5
BRR014 Barrett Esophagus 65 2.667
6
ESP020 Esophageal Atresia 62 2.667
7
VCT001 Vacterl Association 42 2.667
8
P VNT002 Ventricular Septal Defect 60 2.639
9
GST019 Gastrointestinal Stromal Tumor 78 2.607
10
NNS002 Nonspecific Interstitial Pneumonia 45 2.607
11
DDN011 Duodenal Atresia 50 1.962
12
VTR016 Vater/vacterl Association 50 1.935
13
IDP092 Idiopathic/heritable Pulmonary Arterial Hypertension 25 1.935
14
c PYL011 Pyloric Stenosis, Infantile Hypertrophic, 5 12 1.935
15
P HYP055 Hypoplastic Left Heart Syndrome 63 1.903
16
ANS023 Anus, Imperforate 56 1.903
17
PNC118 Pancreas, Annular 42 1.903
18
PLL001 Pallister-Hall Syndrome 64 1.817
19
c DPH024 Diaphragmatic Hernia, Congenital 63 1.817
20
P ATR010 Atrial Heart Septal Defect 60 1.817
21
P PTN014 Patent Ductus Arteriosus 1 60 1.817
22
P FNG006 Feingold Syndrome 1 55 1.817
23
VLV047 Volvulus of Midgut 49 1.817
24
HRN026 Hernia, Hiatus 47 1.817
25
INT060 Intestinal Atresia 40 1.817
26
NNT004 Neonatal Respiratory Failure 36 1.817
27
P LNG032 Lung Cancer 98 0.131
28
P RSP003 Respiratory Failure 74 0.117
29
P RHB003 Rhabdomyosarcoma 63 0.102
30
BRS099 Breast Ductal Carcinoma 62 0.102
31
P CLR023 Colorectal Cancer 99 0.083
32
P MDL005 Medulloblastoma 77 0.083
33
P RTN024 Retinoblastoma 73 0.083
34
GST092 Gastroesophageal Reflux 67 0.083
35
c SML038 Small Cell Cancer of the Lung 65 0.083
36
P PLM036 Pulmonary Fibrosis 65 0.083
37
P ADN016 Adenocarcinoma 64 0.083
38
CHL068 Cholestasis 61 0.083
39
LNG099 Lung Disease 60 0.083
40
BRN056 Bronchopulmonary Dysplasia 57 0.083
41
GST050 Gastrointestinal System Disease 56 0.083
42
GST037 Gastroparesis 54 0.083
43
c FML008 Familial Retinoblastoma 53 0.083
44
PLY150 Polykaryocytosis Inducer 31 0.083
45
ATR053 Atresia of Urethra 20 0.083
46
P HPT023 Hepatocellular Carcinoma 100 0.059
47
P PRS040 Prostate Cancer 97 0.059
48
ESP021 Esophageal Cancer 90 0.059
49
P GST053 Gastric Cancer 83 0.059
50
P ATX030 Ataxia-Telangiectasia 82 0.059
51
c FNC027 Fanconi Anemia, Complementation Group a 81 0.059
52
P LNG064 Lung Cancer Susceptibility 3 78 0.059
53
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.059
54
P HRT032 Heart Disease 75 0.059
55
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.059
56
P OST002 Osteoporosis 74 0.059
57
BSL036 Basal Cell Nevus Syndrome 73 0.059
58
DFC004 Deficiency Anemia 70 0.059
59
P PNM007 Pneumonia 68 0.059
60
c BSL007 Basal Cell Carcinoma 68 0.059
61
c RHB024 Rhabdomyosarcoma 2 67 0.059
62
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.059
63
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.059
64
CLF027 Cleft Palate, Isolated 64 0.059
65
P MST009 Mastocytosis 64 0.059
66
P GLM045 Glioma 63 0.059
67
P ESP024 Esophagitis 62 0.059
68
MDD011 Mood Disorder 62 0.059
69
SPP011 Suppression of Tumorigenicity 12 59 0.059
70
THY029 Thyroid Carcinoma 59 0.059
71
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.059
72
P BPL003 Bipolar Disorder 56 0.059
73
SFT003 Soft Tissue Sarcoma 56 0.059
74
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.059
75
P ATR001 Atrioventricular Septal Defect 55 0.059
76
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.059
77
TND005 Tendinitis 54 0.059
78
PPT001 Peptic Esophagitis 52 0.059
79
TLN003 Telangiectasis 52 0.059
80
CLR109 Colorectal Adenocarcinoma 51 0.059
81
P OMP004 Omphalocele 50 0.059
82
HRT011 Heart Septal Defect 50 0.059
83
CYS002 Cystic Lymphangioma 48 0.059
84
HLX001 Helix Syndrome 47 0.059
85
CHR074 Choriocarcinoma 47 0.059
86
PLY012 Polyhydramnios 46 0.059
87
MGC001 Megacolon 46 0.059
88
GLL048 Glial Tumor 45 0.059
89
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.059
90
TND004 Tendinopathy 43 0.059
91
c MJR024 Major Affective Disorder 9 41 0.059
92
P HYP009 Hypertrophic Pyloric Stenosis 41 0.059
93
KLD004 Keloid Disorder 40 0.059
94
c MJR022 Major Affective Disorder 8 38 0.059
95
KLD003 Keloid Formation 38 0.059
96
c PLM167 Pulmonary Venoocclusive Disease 2, Autosomal Recessive 37 0.059
97
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 33 0.059
98
ERL051 Early Response to Neural Induction Gene 10 0.059
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