Search results for LMX1B

205 hits were found for LMX1B

# Family MCID Name MIFTS Score
1
NLP001 Nail-Patella Syndrome 63 75.350
2
c FCL091 Focal Segmental Glomerulosclerosis 10 27 27.293
3
P NPH012 Nephrotic Syndrome 62 25.614
4
P KDN018 Kidney Disease 72 16.690
5
P ERL057 Early Infantile Epileptic Encephalopathy 61 15.625
6
DRV001 Dravet Syndrome 70 15.625
7
P OPN001 Open-Angle Glaucoma 55 14.636
8
P FCL005 Focal Segmental Glomerulosclerosis 57 13.956
9
RNL078 Renal Dysplasia 46 13.021
10
INT323 Intraocular Pressure Quantitative Trait Locus 63 12.757
11
LPD004 Lipoid Nephrosis 44 12.280
12
GNT031 Genitopatellar Syndrome 42 11.111
13
P PRK057 Parkinson Disease, Late-Onset 79 10.915
14
P ATT013 Attention Deficit-Hyperactivity Disorder 66 10.784
15
SDD001 Sudden Infant Death Syndrome 60 10.266
16
P MTC133 Mitochondrial Myopathy 51 9.961
17
c ART144 Arthrogryposis, Distal, Type 1a 60 9.820
18
KRT019 Keratitis, Hereditary 66 9.820
19
c DVL035 Developmental and Epileptic Encephalopathy 4 38 8.681
20
STX005 Stxbp1 Encephalopathy 23 8.681
21
c GLC092 Glaucoma, Primary Open Angle 61 8.426
22
P ALP004 Alport Syndrome 70 8.350
23
9Q3002 9q33.3q34.11 Microdeletion Syndrome 19 7.904
24
P ANT088 Anterior Segment Dysgenesis 53 7.143
25
PRS055 Pierson Syndrome 54 7.085
26
c ATS018 Autosomal Recessive Alport Syndrome 42 7.085
27
P AXN002 Axenfeld-Rieger Syndrome 62 7.085
28
c FML015 Familial Nephrotic Syndrome 47 7.085
30
CNT097 Central Hypoventilation Syndrome, Congenital 70 6.944
31
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 53 6.944
32
DNY001 Denys-Drash Syndrome 57 6.944
33
P NNP021 Nanophthalmos 40 6.944
34
P GLL032 Galloway-Mowat Syndrome 47 6.944
35
DPN005 Du Pan Syndrome 47 6.944
36
SCH016 Schimke Immunoosseous Dysplasia 53 6.944
37
FRS002 Frasier Syndrome 54 6.944
38
DSS008 Disease of Mental Health 74 6.944
39
PRT251 Proteinuria, Chronic Benign 58 3.360
40
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 35 2.598
41
c NPH049 Nephrotic Syndrome, Type 2 52 2.514
42
END086 End Stage Renal Disease 54 2.236
43
SLC010 Salcedo Syndrome 10 2.044
44
OCL006 Ocular Hypertension 53 1.755
45
P ATS364 Autism 72 1.573
46
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.330
47
HLX001 Helix Syndrome 47 1.230
48
IRN008 Iron Overload in Africa 51 1.189
49
RJS001 Ruijs-Aalfs Syndrome 47 1.189
50
HPT079 Hepatoid Adenocarcinoma 39 1.189
51
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 1.189
52
c HPT073 Hepatitis C Virus 71 1.189
53
P HPT023 Hepatocellular Carcinoma 95 1.189
54
ADL096 Adult Hepatocellular Carcinoma 60 1.189
55
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 1.189
56
PDT042 Pediatric Hepatocellular Carcinoma 50 1.189
57
PTY007 Pityriasis Rotunda 26 1.189
58
FBR086 Fibrolamellar Carcinoma 59 1.189
59
HPT011 Hepatocellular Clear Cell Carcinoma 45 1.189
60
c NPH055 Nephrotic Syndrome, Type 1 52 1.177
61
c CHR684 Chronic Kidney Disease 74 1.177
62
ADR040 Adrenal Gland Pheochromocytoma 45 1.138
63
P PHC003 Pheochromocytoma 70 1.138
64
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.117
65
P OVR042 Ovarian Cancer 88 1.095
66
GLM045 Glioma 62 1.095
67
GLL048 Glial Tumor 52 1.095
68
HYP266 Hypoxia 56 1.095
69
LRY018 Laryngeal Squamous Cell Carcinoma 47 1.072
70
SQM006 Squamous Cell Carcinoma 59 1.072
71
P SCH015 Schizophrenia 74 1.022
72
GLM044 Glomerular Disease 34 1.022
73
FBR012 Fabry Disease 71 0.994
74
RNL025 Renal Hypoplasia 46 0.964
75
c VSC019 Vesicoureteral Reflux 1 56 0.964
76
HRM002 Hermaphroditism 35 0.964
77
c 46X011 46, Xy Disorders of Sexual Development 20 0.964
78
ESP021 Esophageal Cancer 84 0.931
79
PLY150 Polykaryocytosis Inducer 29 0.931
80
GDP001 Goodpasture Syndrome 55 0.931
81
P MJR001 Major Depressive Disorder 68 0.931
82
P CRN037 Craniosynostosis 67 0.931
83
MNT002 Mental Depression 56 0.931
84
DPR016 Depression 65 0.931
85
LMY003 Leiomyomatosis 43 0.931
86
INT020 Intravenous Leiomyomatosis 36 0.931
87
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.848
88
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.848
89
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.848
90
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.848
91
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.848
92
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.848
93
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.848
94
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.848
95
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.848
96
P MMB011 Membranous Nephropathy 50 0.848
97
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.848
98
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 56 0.848
99
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.848
100
P MVM001 Movement Disease 61 0.848
101
SYN005 Synostosis 43 0.848
102
P GLM007 Glomerulonephritis 59 0.848
103
P ECT006 Ectodermal Dysplasia 62 0.848
104
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 0.848
105
STX004 Stxbp1 Encephalopathy with Epilepsy 14 0.848
106
PRX035 Paroxysmal Dyskinesia 30 0.848
107
GNT182 Genetic Nephrotic Syndrome 11 0.848
109
c TBR025 Tuberous Sclerosis 1 84 0.790
110
P TBR001 Tuberous Sclerosis 69 0.790
111
P BRS047 Breast Cancer 97 0.779
112
P FML018 Familial Mediterranean Fever 73 0.649
113
BRC012 Brucellosis 66 0.649
114
RNL077 Renal Fibrosis 46 0.564
115
P DSR090 Disorder of Sexual Development 45 0.551
116
P PNC035 Pancreatic Cancer 86 0.551
117
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.423
118
URT010 Ureteral Obstruction 45 0.423
119
P RSP003 Respiratory Failure 74 0.315
120
P SLP006 Sleep Apnea 69 0.282
121
c WLM013 Wilms Tumor 1 65 0.282
122
DPH001 Diphtheria 59 0.282
123
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.244
124
SKL017 Skeletal Dysplasias 41 0.244
125
CLL035 Collagen Type Iii Glomerulopathy 14 0.244
126
AST006 Astigmatism 46 0.199
127
AMB002 Amblyopia 49 0.199
128
SPP007 Suppression Amblyopia 38 0.199
129
P LFT003 Left Ventricular Noncompaction 57 0.199
130
CLB002 Clubfoot 51 0.199
131
P HYP086 Hypothyroidism 69 0.199
132
P HYP061 Hypertrophic Cardiomyopathy 69 0.199
133
P SZR006 Seizure Disorder 69 0.199
134
48X005 48,xyyy 39 0.199
135
CRB053 Cerebellar Agenesis 16 0.199
136
P MTC069 Mitochondrial Disorders 57 0.199
137
BSL036 Basal Cell Nevus Syndrome 73 0.141
138
CRN270 Coronary Artery Dissection, Spontaneous 32 0.141
139
BRT005 Barth Syndrome 55 0.141
140
AGN016 Aging 54 0.141
141
c BRN108 Branchiootic Syndrome 1 63 0.141
143
ANX010 Anxiety 70 0.141
144
TBL029 Tubulin, Beta 28 0.141
145
FCL009 Focal Dermal Hypoplasia 64 0.141
146
ATS010 Autosomal Recessive Disease 42 0.141
147
c PRC016 Pre-Eclampsia 64 0.141
148
RCK004 Rickets 65 0.141
149
P PRK039 Parkinsonism 55 0.141
150
P PLY014 Polycystic Kidney Disease 71 0.141
151
SPN221 Spina Bifida Occulta 39 0.141
152
OBS002 Obsessive-Compulsive Disorder 68 0.141
153
STH001 Saethre-Chotzen Syndrome 66 0.141
154
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.141
155
c GLC097 Glaucoma 3, Primary Congenital, a 57 0.141
156
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.141
157
SMT008 Smith-Magenis Syndrome 53 0.141
158
P MRG008 Meier-Gorlin Syndrome 1 55 0.141
159
c ATS007 Autism Spectrum Disorder 72 0.141
160
PNG002 Pain Agnosia 51 0.141
161
P LYS001 Loeys-Dietz Syndrome 65 0.141
162
P SCL018 Scoliosis 57 0.141
163
P LRS001 Larsen Syndrome 61 0.141
164
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 54 0.141
165
c MYT021 Myotonic Dystrophy 1 67 0.141
166
PCT003 Pectus Excavatum 43 0.141
167
FBR032 Fibromuscular Dysplasia 47 0.141
168
NRL016 Neural Tube Defects 81 0.141
169
c MJR024 Major Affective Disorder 9 40 0.141
170
c MJR022 Major Affective Disorder 8 37 0.141
171
c GLC041 Glaucoma 1, Open Angle, a 34 0.141
172
P LSS002 Lissencephaly 53 0.141
173
c PRM032 Primary Congenital Glaucoma 40 0.141
174
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.141
175
P MYP006 Myopia 55 0.141
176
IGG001 Iga Glomerulonephritis 50 0.141
177
P VSC007 Vascular Disease 62 0.141
178
c BSL007 Basal Cell Carcinoma 68 0.141
179
P EHL001 Ehlers-Danlos Syndrome 57 0.141
180
P SDR002 Siderosis 42 0.141
181
P LKM002 Leukemia 66 0.141
182
P ART023 Arthropathy 60 0.141
183
P BPL003 Bipolar Disorder 56 0.141
184
P TRT010 Teratoma 50 0.141
185
CNS004 Constipation 56 0.141
186
BRS051 Breast Disease 58 0.141
187
c RTN041 Retinitis Pigmentosa 11 43 0.141
188
P PLY006 Polydactyly 58 0.141
189
NRM005 Neuromuscular Disease 63 0.141
190
SYN036 Syncope 44 0.141
191
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.141
192
c NNS007 Nonsyndromic Deafness 32 0.141
193
P MYP004 Myopathy 67 0.141
194
P EYD002 Eye Disease 57 0.141
195
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.141
196
P MYT002 Myotonic Dystrophy 51 0.141
197
ETN001 Eating Disorder 59 0.141
198
c LKM005 Leukemia, T-Cell, Chronic 33 0.141
199
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.141
200
ATS117 Autosomal Recessive Nail Dysplasia 12 0.141
201
GNT082 Genetic Neuromuscular Disease 10 0.141
202
CNG506 Congenital Amyoplasia 27 0.141
203
LYS029 Lysosomal Disease 30 0.141
204
MCR103 Microtia 40 0.141
205
CNG587 Congenital Limb Malformation 12 0.141
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