Search results for lama1

145 hits were found for lama1

# Family MCID Name MIFTS Score
1
PRT101 Poretti-Boltshauser Syndrome 32 53.439
2
P MYP006 Myopia 55 17.355
3
P MSC005 Muscular Dystrophy 66 12.525
4
P STR020 Strabismus 56 11.265
5
NRM005 Neuromuscular Disease 62 11.265
6
FND002 Fundus Dystrophy 54 9.510
7
CHR211 Chromosome 18p Deletion Syndrome 38 8.965
8
MSC162 Muscular Dystrophy, Congenital Merosin-Deficient, 1a 55 8.364
9
P CNG001 Congenital Myasthenic Syndrome 68 8.178
10
MSC164 Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency 47 7.965
11
HTC003 Hutchinson-Gilford Progeria Syndrome 65 7.965
12
AFR001 African Histoplasmosis 22 7.965
13
RTN020 Retinal Vascular Disease 45 1.986
14
c INH030 Inherited Retinal Disorder 28 1.545
15
c MYP127 Myopia 2, Autosomal Dominant 26 1.443
16
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 1.308
17
c CLR087 Colorectal Cancer 12 34 1.308
18
GST103 Gastric Cancer, Hereditary Diffuse 68 1.308
19
SML009 Small Intestine Adenocarcinoma 57 1.308
20
KRT009 Keratosis 52 1.306
21
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.261
23
P TCD001 Tic Disorder 50 1.191
24
DGN002 Degenerative Myopia 31 1.165
25
P MCR129 Microvascular Complications of Diabetes 1 67 1.137
26
c MCR112 Microvascular Complications of Diabetes 2 42 1.137
27
c MCR115 Microvascular Complications of Diabetes 5 65 1.137
28
HYP066 Hyperglycemia 60 1.137
29
c PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 39 1.108
30
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.108
31
SQM006 Squamous Cell Carcinoma 59 1.108
32
P RTN018 Retinal Disease 53 1.108
33
P VTR007 Vitreoretinopathy 45 1.108
34
c MYP018 Myopia 6 29 1.040
35
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.040
36
P MYP137 Myopia 1, X-Linked 18 1.000
37
c MYP044 Myopia 10 18 1.000
38
c HRD026 Hereditary Ataxia 46 1.000
39
SKN016 Skin Disease 63 1.000
40
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.952
41
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.952
42
AGN016 Aging 53 0.858
43
LNG039 Lung Squamous Cell Carcinoma 57 0.844
44
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.844
45
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.844
46
P BRS047 Breast Cancer 97 0.786
47
P LNG021 Lung Occult Small Cell Carcinoma 20 0.755
48
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.755
49
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.755
50
P SCH015 Schizophrenia 74 0.573
51
P PNC035 Pancreatic Cancer 87 0.573
52
PRT251 Proteinuria, Chronic Benign 58 0.543
53
CLN015 Colon Adenocarcinoma 64 0.534
54
EMB004 Embryonal Carcinoma 55 0.399
55
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.378
56
c GLM043 Glioma Susceptibility 9 30 0.378
57
c GLM025 Glioma Susceptibility 2 30 0.378
58
c GLM047 Glioma Susceptibility 3 32 0.378
59
MNN043 Meningioma, Familial 79 0.378
60
P GLM040 Glioma Susceptibility 1 70 0.378
61
P OLG002 Oligodendroglioma 66 0.378
62
BRS099 Breast Ductal Carcinoma 61 0.378
63
GLM045 Glioma 62 0.378
64
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.369
65
P MYP004 Myopathy 67 0.369
66
P MSC003 Muscular Atrophy 52 0.369
67
c CNG112 Congenital Muscular Dystrophy Type 1a 32 0.369
68
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.337
69
P ANT088 Anterior Segment Dysgenesis 54 0.337
70
P CTR002 Cataract 59 0.337
71
APR001 Apraxia 51 0.301
72
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.301
73
OCL069 Ocular Motor Apraxia 57 0.301
74
P PLM036 Pulmonary Fibrosis 65 0.301
75
CHR074 Choriocarcinoma 46 0.261
76
P ALZ034 Alzheimer Disease 87 0.213
77
DWN001 Down Syndrome 70 0.213
78
c SYS001 Systemic Lupus Erythematosus 85 0.213
79
CLB010 Coloboma of Macula 53 0.213
80
c SCH079 Schizophrenia 1 44 0.213
81
c BRN108 Branchiootic Syndrome 1 63 0.213
82
ATM095 Autoimmune Disease 61 0.213
83
c PRC016 Pre-Eclampsia 64 0.213
84
P MLN008 Melanoma 75 0.213
85
18P001 18p Deletion Syndrome 13 0.213
86
P LPS004 Lupus Erythematosus 61 0.213
87
CHR178 Chromosomal Triplication 33 0.213
88
GRW007 Growth Hormone Deficiency 47 0.213
89
P PRS124 Presynaptic Congenital Myasthenic Syndromes 38 0.213
90
P HYP265 Hypotonia 42 0.213
91
P SCL048 Sclerosteosis 58 0.151
92
P ATR011 Atrial Fibrillation 66 0.151
93
ORL015 Oral Squamous Cell Carcinoma 43 0.151
94
ATH013 Atherosclerosis Susceptibility 63 0.151
95
c WLM013 Wilms Tumor 1 65 0.151
96
P ATS364 Autism 72 0.151
97
P OVR042 Ovarian Cancer 88 0.151
98
P RTN024 Retinoblastoma 72 0.151
99
P HRS035 Hirschsprung Disease 1 66 0.151
100
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.151
101
OST159 Osteogenic Sarcoma 66 0.151
102
P CLR023 Colorectal Cancer 100 0.151
103
ACT088 Acute Insulin Response 39 0.151
104
LMB002 Lambert-Eaton Myasthenic Syndrome 51 0.151
105
P LSS002 Lissencephaly 52 0.151
106
P JBR020 Joubert Syndrome 1 74 0.151
107
PNT009 Pontine Tegmental Cap Dysplasia 34 0.151
108
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.151
109
HYP748 Hypertelorism 46 0.151
110
CHD004 Chudley-Mccullough Syndrome 47 0.151
111
P BND020 Bone Disease 60 0.151
112
P CRB045 Cerebellar Hypoplasia 40 0.151
113
P CHR084 Chromosomal Disease 35 0.151
114
OST003 Osteonecrosis 60 0.151
115
THR024 Thrombosis 56 0.151
116
NNL006 Non-Alcoholic Steatohepatitis 54 0.151
117
CLR108 Colorectal Adenoma 63 0.151
118
TBL035 Tubulinopathy 34 0.151
119
MCR099 Microlissencephaly 39 0.151
120
CRB037 Cerebral Palsy 66 0.151
121
P BNG030 Benign Ependymoma 51 0.151
122
P TRN020 Turner Syndrome 67 0.151
123
CLR030 Clear Cell Renal Cell Carcinoma 53 0.151
124
CLL010 Cellular Ependymoma 58 0.151
125
ANP006 Anaplastic Ependymoma 46 0.151
126
ADN018 Adenoma 58 0.151
127
FRZ001 Frozen Shoulder 54 0.151
128
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.151
129
P LVR013 Liver Disease 68 0.151
130
PTS001 Patau Syndrome 55 0.151
131
LGN002 Legionellosis 61 0.151
132
P GND004 Gonadal Dysgenesis 46 0.151
133
PRT037 Pertussis 49 0.151
134
P CWD010 Cowden Syndrome 70 0.151
135
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.151
136
SPC005 Speech Disorder 46 0.151
137
OST012 Osteoarthritis 77 0.151
138
CYT002 Cytokine Deficiency 43 0.151
139
FTT001 Fatty Liver Disease 61 0.151
140
ORL011 Oral Cancer 60 0.151
141
HMM003 Hemimegalencephaly 53 0.151
142
c MNS008 Monosomy 21 25 0.151
143
P DNC006 Diencephalic-Mesencephalic Junction Dysplasia 20 0.151
144
P MGL013 Megalencephaly 46 0.151
145
RHM015 Rhombencephalosynapsis 29 0.151
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