Search results for fbln5

152 hits were found for fbln5

# Family MCID Name MIFTS Score
3
c CTS031 Cutis Laxa, Autosomal Dominant 2 41 34.838
4
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 45 32.182
5
P CTS001 Cutis Laxa 64 30.961
6
c ATS393 Autosomal Recessive Cutis Laxa Type I 49 28.655
7
c CTS045 Cutis Laxa, Autosomal Dominant 1 52 28.409
8
P NRP001 Neuropathy 59 15.030
10
ART016 Aortic Aneurysm 68 13.047
11
P PLV020 Pelvic Organ Prolapse 57 12.360
12
P PLM034 Pulmonary Emphysema 58 11.998
13
ING001 Inguinal Hernia 59 11.979
14
TTH006 Tooth Disease 51 11.165
15
P CHR071 Charcot-Marie-Tooth Disease 64 11.142
16
SPR004 Supravalvular Aortic Stenosis 57 10.097
17
CST001 Costello Syndrome 68 10.097
18
ANR040 Aneurysm 60 9.731
19
P SCL018 Scoliosis 57 9.541
20
ART074 Aortic Dissection 53 9.541
21
CHR629 Charcot-Marie-Tooth Disease and Deafness 55 9.388
22
PNM008 Pneumothorax 54 9.388
23
P EYD002 Eye Disease 57 9.388
24
CNN005 Connective Tissue Disease 66 9.388
25
TRC007 Tricuspid Valve Prolapse 35 8.297
26
P PRX014 Proximal Spinal Muscular Atrophy 44 8.152
27
ART001 Arterial Tortuosity Syndrome 64 7.781
28
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 50 7.654
29
c ACQ027 Acquired Cutis Laxa 25 7.654
30
c CTS038 Cutis Laxa, Autosomal Recessive, Type Iia 46 7.564
31
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 7.564
32
GRD005 Geroderma Osteodysplasticum 48 7.501
33
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 45 7.501
34
DYN002 Doyne Honeycomb Retinal Dystrophy 44 7.347
35
OCC006 Occipital Horn Syndrome 53 7.347
36
c CTS023 Cutis Laxa, Autosomal Recessive, Type Iib 43 7.347
37
BLD045 Bladder Diverticulum 39 7.347
38
c ATS392 Autosomal Recessive Cutis Laxa Type Iii 48 7.347
39
URT023 Ureteric Orifice Cancer 27 7.347
40
ATS391 Autosomal Recessive Cutis Laxa Type Ii Classic Type 35 7.347
41
PHC002 Phacogenic Glaucoma 26 7.347
42
MDD015 Mid-Dermal Elastolysis 25 7.347
43
c CRD090 Cardiomyopathy, Dilated, 1l 41 6.638
44
BSL037 Basal Laminar Drusen 41 6.638
45
MCS006 Macs Syndrome 57 6.638
46
P LYS001 Loeys-Dietz Syndrome 65 6.638
47
RTN006 Retinal Drusen 34 6.638
48
P ENT005 Entropion 34 6.638
49
LCR013 Lacrimal Duct Defect 40 1.659
50
CNJ007 Conjunctivochalasis 38 1.659
51
FND002 Fundus Dystrophy 54 1.514
52
P PNC035 Pancreatic Cancer 87 1.176
53
c VSC019 Vesicoureteral Reflux 1 56 1.138
54
P URN019 Urinary Tract Infection 48 1.138
55
c ACT068 Acute Cystitis 60 1.138
56
P MCR010 Microcephaly 59 1.108
57
P VNT002 Ventricular Septal Defect 58 1.039
58
HRT011 Heart Septal Defect 49 1.039
59
LMY002 Leiomyoma 51 1.039
60
PYL006 Pyloric Stenosis 48 1.039
61
FTL021 Fetal Macrosomia 40 1.039
62
P LMY004 Leiomyosarcoma 62 0.998
63
P PLY019 Polyneuropathy 52 0.998
65
CHL065 Cholangiocarcinoma 57 0.949
66
INT079 Intrahepatic Cholangiocarcinoma 51 0.949
67
WRN004 Wrinkly Skin Syndrome 37 0.862
68
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.811
69
P HPT023 Hepatocellular Carcinoma 95 0.804
70
END057 Endometrial Cancer 76 0.733
71
P END044 Endometriosis 62 0.733
72
P VSC011 Vasculitis 61 0.733
73
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 53 0.709
74
c ART101 Aortic Valve Disease 2 65 0.709
75
P ART018 Aortic Valve Insufficiency 52 0.709
76
P LNG021 Lung Occult Small Cell Carcinoma 20 0.691
77
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.691
78
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.691
79
HYP266 Hypoxia 56 0.686
80
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.616
81
P BRS047 Breast Cancer 97 0.602
82
P OVR042 Ovarian Cancer 88 0.574
83
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.574
84
OVR094 Ovarian Epithelial Cancer 39 0.509
85
CHR177 Chromophobe Renal Cell Carcinoma 54 0.471
86
INS001 Insulinoma 59 0.434
88
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.406
89
IRN008 Iron Overload in Africa 50 0.399
90
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.399
91
c HPT073 Hepatitis C Virus 70 0.399
92
RJS001 Ruijs-Aalfs Syndrome 47 0.399
93
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.399
94
ADL096 Adult Hepatocellular Carcinoma 60 0.399
95
HPT079 Hepatoid Adenocarcinoma 39 0.399
96
PDT042 Pediatric Hepatocellular Carcinoma 51 0.399
97
FBR086 Fibrolamellar Carcinoma 59 0.399
98
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.399
99
PTY007 Pityriasis Rotunda 27 0.399
100
P PRS040 Prostate Cancer 95 0.376
101
ATS010 Autosomal Recessive Disease 42 0.376
102
DMY004 Demyelinating Disease 50 0.376
103
P VSC007 Vascular Disease 62 0.343
104
BRN056 Bronchopulmonary Dysplasia 57 0.266
106
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.217
107
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.217
108
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.217
109
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.217
110
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.217
111
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.217
112
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.217
113
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.217
114
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.217
115
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.217
116
P LVR013 Liver Disease 68 0.217
117
FTT001 Fatty Liver Disease 61 0.217
118
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.217
119
RRG043 Rare Genetic Skin Disease 17 0.217
120
P OVR082 Overgrowth Syndrome 41 0.217
121
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.153
122
PRT251 Proteinuria, Chronic Benign 58 0.153
123
P STR022 Stargardt Disease 61 0.153
124
P LYM118 Lymphoma 66 0.153
125
ATH013 Atherosclerosis Susceptibility 63 0.153
126
c ART115 Aortic Valve Disease 1 72 0.153
127
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.153
128
NRL016 Neural Tube Defects 80 0.153
129
c STR084 Stargardt Disease 1 54 0.153
130
c EXD008 Exudative Vitreoretinopathy 1 71 0.153
131
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.153
132
ADR016 Adrenal Cortical Carcinoma 61 0.153
133
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.153
134
c NPH019 Nephronophthisis 1 50 0.153
135
P RTN008 Retinitis Pigmentosa 79 0.153
136
P STR020 Strabismus 56 0.153
137
P CNR004 Cone-Rod Dystrophy 2 74 0.153
138
P BND020 Bone Disease 60 0.153
139
DFF005 Diffuse Large B-Cell Lymphoma 55 0.153
140
NRR001 Neuroretinitis 42 0.153
141
P MYP004 Myopathy 67 0.153
142
ADR004 Adrenal Cortical Adenocarcinoma 38 0.153
143
P ADL010 Adult Respiratory Distress Syndrome 70 0.153
144
JPN002 Japanese Encephalitis 61 0.153
145
OLG003 Oligohydramnios 50 0.153
146
RTN023 Retinitis 45 0.153
147
P DBT009 Diabetes Mellitus 67 0.153
148
P ENC004 Encephalitis 61 0.153
149
MCH006 Mechanical Strabismus 40 0.153
150
P BCL017 B-Cell Lymphoma 57 0.153
151
P PRD008 Periodontitis 63 0.153
152
c HRD088 Hereditary Neuropathies 34 0.153
Content
Loading form....