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Search results for fn1

181 hits were found for fn1

# Family MCID Name MIFTS Score
1
SPN360 Spondylometaphyseal Dysplasia, Corner Fracture Type 38 3.614
2
P GLM015 Glomerulopathy with Fibronectin Deposits 2 34 3.468
3
P CLR023 Colorectal Cancer 99 3.385
4
P LNG032 Lung Cancer 98 3.151
5
P BRS047 Breast Cancer 97 2.684
6
P OVR042 Ovarian Cancer 88 2.663
7
P PRS040 Prostate Cancer 97 2.382
8
P BLD134 Bladder Cancer 79 2.382
9
c PRC016 Pre-Eclampsia 63 2.113
10
P WRD001 Waardenburg's Syndrome 59 2.089
11
P FBR017 Fibrosarcoma 56 2.089
12
P PNC035 Pancreatic Cancer 84 2.063
13
CYS001 Cystic Fibrosis 81 2.063
14
P HRT032 Heart Disease 75 2.063
15
P MYC007 Myocardial Infarction 70 2.063
16
CNG034 Congestive Heart Failure 69 2.063
17
P PLM037 Pulmonary Hypertension 67 2.063
18
P PSR002 Psoriasis 62 2.063
19
P EHL001 Ehlers-Danlos Syndrome 58 2.063
20
P GLM007 Glomerulonephritis 57 2.063
21
DSS009 Disseminated Intravascular Coagulation 57 2.063
22
c ACT075 Acute Myocardial Infarction 57 2.063
23
P KRT007 Keratoconus 50 2.063
24
c CHR684 Chronic Kidney Disease 70 1.916
25
c AMY091 Amyotrophic Lateral Sclerosis 1 89 1.684
26
MYL069 Myeloma, Multiple 85 1.684
28
c HYP595 Hypertension, Essential 84 1.684
29
c DLT002 Dilated Cardiomyopathy 79 1.684
30
P NNN008 Noonan Syndrome 1 76 1.684
31
c ART115 Aortic Valve Disease 1 75 1.684
32
P APL001 Aplastic Anemia 74 1.684
33
P KDN018 Kidney Disease 72 1.684
34
P NRB001 Neuroblastoma 72 1.684
35
c LKM063 Leukemia, Chronic Myeloid 72 1.684
36
P HYP061 Hypertrophic Cardiomyopathy 70 1.684
37
P PNM007 Pneumonia 68 1.684
38
P SYS005 Systemic Scleroderma 68 1.684
39
P MYC084 Mycobacterium Tuberculosis 1 68 1.684
40
P MSC005 Muscular Dystrophy 66 1.684
41
GLN010 Glanzmann Thrombasthenia 66 1.684
42
P VSC007 Vascular Disease 63 1.684
43
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.684
44
LNG099 Lung Disease 60 1.684
45
STR039 Sturge-Weber Syndrome 60 1.684
46
VRC005 Varicose Veins 60 1.684
47
P CTR002 Cataract 60 1.684
48
P SYP003 Syphilis 58 1.684
49
DST005 Diastrophic Dysplasia 58 1.684
50
EXT034 Extrinsic Allergic Alveolitis 58 1.684
51
P PNM006 Pneumoconiosis 56 1.684
52
NPH009 Nephrolithiasis 55 1.684
53
P EPD016 Epidermolysis Bullosa 53 1.684
54
CLC001 Calciphylaxis 51 1.684
55
c SVR005 Severe Pre-Eclampsia 50 1.684
56
P GNG025 Gingival Fibromatosis 50 1.684
57
RNL077 Renal Fibrosis 47 1.684
58
EXS001 Exostosis 46 1.684
59
MSN001 Mesangial Proliferative Glomerulonephritis 45 1.684
60
DBT008 Diabetic Angiopathy 44 1.684
61
c SCN006 Secondary Syphilis 40 1.684
62
PRR004 Preretinal Fibrosis 37 1.684
63
INT016 Intraductal Papilloma 36 1.684
64
PLS026 Plasma Fibronectin Deficiency 16 1.264
65
AMB001 Amebiasis 55 1.232
66
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.191
67
c LKM061 Leukemia, Acute Myeloid 84 1.191
68
SQM013 Squamous Cell Carcinoma, Head and Neck 80 1.191
69
P RTN008 Retinitis Pigmentosa 79 1.191
70
P LNG064 Lung Cancer Susceptibility 3 78 1.191
71
PLM134 Pulmonary Fibrosis, Idiopathic 77 1.191
72
BRT054 Brittle Bone Disorder 72 1.191
73
ODN023 Odontochondrodysplasia 68 1.191
74
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 1.191
75
P CNG001 Congenital Myasthenic Syndrome 66 1.191
76
c HRD010 Hereditary Spastic Paraplegia 66 1.191
77
c GLC092 Glaucoma, Primary Open Angle 62 1.191
78
P BTH005 Bethlem Myopathy 1 62 1.191
79
P KLL001 Kallmann Syndrome 61 1.191
80
MCK005 Mckusick-Kaufman Syndrome 61 1.191
81
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 61 1.191
82
DCB001 Decubitus Ulcer 61 1.191
83
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 60 1.191
84
SPP011 Suppression of Tumorigenicity 12 59 1.191
85
EYD002 Eye Disease 58 1.191
86
P PRP019 Peripheral Nervous System Disease 58 1.191
87
FND002 Fundus Dystrophy 55 1.191
88
CHR100 Chronic Ulcer of Skin 55 1.191
89
URN010 Urinary Tract Obstruction 55 1.191
90
GLS001 Gliosarcoma 54 1.191
91
PRT082 Preterm Premature Rupture of the Membranes 54 1.191
92
VGN023 Vaginitis 54 1.191
93
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.191
94
EPD077 Epidermolysis Bullosa Junctionalis with Pyloric Atresia 54 1.191
95
DFF036 Differentiated Thyroid Carcinoma 52 1.191
96
c HYP602 Hyperoxaluria, Primary, Type Ii 51 1.191
97
CMB003 Combined T Cell and B Cell Immunodeficiency 49 1.191
98
IMP004 Impetigo 49 1.191
99
NCR007 Necrotizing Fasciitis 48 1.191
100
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 1.191
101
URN009 Urinary System Disease 48 1.191
102
P CRN028 Corneal Ulcer 47 1.191
103
P RNL015 Renal Hypertension 47 1.191
104
RTN020 Retinal Vascular Disease 46 1.191
105
SCL002 Scleredema Adultorum 46 1.191
106
GNG011 Gingival Disease 45 1.191
107
c SPH017 Spherocytosis, Type 5 44 1.191
108
FCH001 Fuchs' Endothelial Dystrophy 44 1.191
109
P CRN024 Corneal Disease 44 1.191
110
URT031 Ureteral Disease 41 1.191
111
c ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 41 1.191
112
MCL003 Macular Holes 40 1.191
113
VTR005 Vitreous Disease 39 1.191
114
VTR003 Vitreous Detachment 39 1.191
115
c HYP507 Hypotrichosis 1 39 1.191
116
RTN002 Retinal Perforation 38 1.191
117
HLZ001 Holzgreve Syndrome 38 1.191
118
VSC012 Vesiculobullous Skin Disease 38 1.191
119
ERY001 Erysipeloid 37 1.191
120
MYC017 Mycobacterium Kansasii 36 1.191
121
c DFN274 Deafness, Autosomal Dominant 56 35 1.191
122
WBR001 Weber Syndrome 35 1.191
123
CRV025 Cervical Incompetence 34 1.191
124
c TYP024 Type Ii Mixed Cryoglobulinemia 34 1.191
125
KDN013 Kidney Hypertrophy 32 1.191
126
STR019 Steroid-Induced Glaucoma 32 1.191
127
RCR001 Recurrent Corneal Erosion 31 1.191
128
TRC001 Trachea Leiomyoma 30 1.191
129
c AMY022 Amyotrophic Lateral Sclerosis Type 5 30 1.191
130
CNV003 Conventional Fibrosarcoma 29 1.191
131
P CRY006 Cryofibrinogenemia 27 1.191
132
HRY002 Hairy Tongue 26 1.191
133
c ATS009 Autosomal Genetic Disease 25 1.191
134
DFF002 Diffuse Pulmonary Fibrosis 25 1.191
135
c EPL093 Epilepsy, Idiopathic Generalized 7 25 1.191
136
CLC064 Calcifying Aponeurotic Fibroma 23 1.191
137
END074 Endocardium Disease 22 1.191
138
ACT041 Acute Diffuse Nephritis 22 1.191
139
CRT003 Cortical Senile Cataract 20 1.191
140
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 49 0.250
141
P NSP012 Nasopharyngeal Carcinoma 66 0.086
142
END086 End Stage Renal Disease 51 0.086
143
ESP021 Esophageal Cancer 90 0.071
144
P GST053 Gastric Cancer 83 0.071
145
P END044 Endometriosis 63 0.071
146
THY029 Thyroid Carcinoma 59 0.071
147
P BCL017 B-Cell Lymphoma 58 0.071
148
ORL015 Oral Squamous Cell Carcinoma 43 0.071
149
c GLM014 Glomerulopathy with Fibronectin Deposits 1 20 0.071
150
c SYS001 Systemic Lupus Erythematosus 86 0.050
151
CRV035 Cervical Cancer 76 0.050
152
P SRC025 Sarcoidosis 1 70 0.050
153
GST040 Gastric Adenocarcinoma 70 0.050
154
P MLN008 Melanoma 69 0.050
155
P HRS035 Hirschsprung Disease 1 65 0.050
156
CLR108 Colorectal Adenoma 64 0.050
157
P ENC018 Encephalopathy 61 0.050
158
SQM006 Squamous Cell Carcinoma 60 0.050
159
MCR013 Microphthalmia 57 0.050
160
BRN056 Bronchopulmonary Dysplasia 57 0.050
161
HYP266 Hypoxia 57 0.050
162
P CHN012 Chondrosarcoma 56 0.050
163
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.050
164
NRN004 Neuroendocrine Tumor 55 0.050
165
DFF005 Diffuse Large B-Cell Lymphoma 55 0.050
166
c MCR113 Microvascular Complications of Diabetes 3 52 0.050
167
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.050
168
P OVR049 Ovarian Disease 52 0.050
169
LMY002 Leiomyoma 52 0.050
170
P IGN003 Iga Nephropathy 1 49 0.050
171
IGG001 Iga Glomerulonephritis 48 0.050
172
PPL002 Papillary Carcinoma 47 0.050
173
c MCR120 Microvascular Complications of Diabetes 7 47 0.050
174
INF058 Inflammatory Myofibroblastic Tumor 45 0.050
175
CHN010 Chondroma 43 0.050
176
P AVS003 Avascular Necrosis 42 0.050
177
SYN031 Synovial Chondromatosis 42 0.050
178
c MCR130 Microvascular Complications of Diabetes 6 41 0.050
179
c MCR133 Microvascular Complications of Diabetes 4 41 0.050
180
PCT001 Pectus Carinatum 35 0.050
181
EXT012 Extraskeletal Chondroma 19 0.050
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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