Search results for hspd1

233 hits were found for hspd1

# Family MCID Name MIFTS Score
1
c LKD008 Leukodystrophy, Hypomyelinating, 4 35 52.065
2
c SPS097 Spastic Paraplegia 13, Autosomal Dominant 42 46.446
3
c SPS023 Spastic Paraplegia 13 20 34.243
4
PLZ002 Pelizaeus-Merzbacher-Like Disease 37 20.461
5
PRP016 Paraplegia 52 16.778
6
c HRD010 Hereditary Spastic Paraplegia 65 15.244
7
P LKD001 Leukodystrophy 58 14.276
8
P HYP700 Hypomyelinating Leukodystrophy 35 13.591
9
P OVR042 Ovarian Cancer 88 13.216
10
RCT015 Reactive Arthritis 60 11.782
11
c TYP008 Type 1 Diabetes Mellitus 77 11.636
12
SDD001 Sudden Infant Death Syndrome 60 11.191
13
c DLT002 Dilated Cardiomyopathy 79 10.464
14
CHL123 Chlamydia 58 10.370
15
P VSC007 Vascular Disease 62 10.284
16
KWS002 Kawasaki Disease 65 10.077
17
P INF037 Inflammatory Bowel Disease 53 10.077
18
P MLT020 Multiple Sclerosis 79 10.077
19
P RHM011 Rheumatoid Arthritis 81 10.077
20
MLR004 Malaria 78 10.077
21
ATM095 Autoimmune Disease 61 10.077
22
c SYS001 Systemic Lupus Erythematosus 86 10.077
23
P UVT001 Uveitis 57 10.077
24
CNN005 Connective Tissue Disease 66 10.077
25
P ART021 Arteriosclerosis 53 10.077
26
MXD005 Mixed Connective Tissue Disease 57 10.077
27
P VSC011 Vasculitis 61 10.077
28
P ART022 Arthritis 70 10.077
29
P MTC069 Mitochondrial Disorders 57 10.077
30
P DBT009 Diabetes Mellitus 67 10.077
31
BCT022 Bacterial Infectious Disease 56 8.435
32
c SPN225 Spondyloarthropathy 1 70 8.374
33
ATH013 Atherosclerosis Susceptibility 63 8.374
34
MTC004 Mitochondrial Encephalomyopathy 43 8.374
35
CYS001 Cystic Fibrosis 77 8.228
36
EPD015 Epidemic Typhus 44 8.228
37
DSS032 Disease by Infectious Agent 55 8.228
38
PLV003 Pelvic Inflammatory Disease 54 8.228
39
P END033 Endocarditis 58 8.228
40
LGN002 Legionellosis 61 8.228
41
BHC003 Behcet Syndrome 71 8.228
42
IMM167 Immune Deficiency Disease 77 8.228
43
P MYC084 Mycobacterium Tuberculosis 1 68 8.228
44
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 8.228
45
ACT049 Acute Disseminated Encephalomyelitis 53 8.228
46
P SLP003 Salpingitis 40 8.228
47
P CRV039 Cervicitis 52 8.228
48
TXC005 Toxic Shock Syndrome 62 8.228
49
URT001 Urethritis 52 8.228
50
PRM236 Primary Biliary Cholangitis 62 8.228
51
LYM017 Lyme Disease 63 8.228
52
VLV010 Vulvovaginitis 42 8.228
53
P MTC133 Mitochondrial Myopathy 51 8.228
54
WHP001 Whipple Disease 45 8.228
55
ORL013 Oral Lichen Planus 45 8.228
56
CHL147 Chlamydia Pneumonia 47 5.964
57
c PNT044 Pontocerebellar Hypoplasia, Type 2a 41 5.818
58
CMP087 Complement Component 7 Deficiency 37 5.818
59
RCK002 Rocky Mountain Spotted Fever 34 5.818
60
ADS001 Adiaspiromycosis 29 5.818
61
PRM025 Primary Bacterial Infectious Disease 29 5.818
62
END014 Endemic Typhus 32 5.818
63
ATM103 Autoimmune Atherosclerosis 19 5.818
64
HMN002 Human Granulocytic Anaplasmosis 31 5.818
65
HMN001 Human Monocytic Ehrlichiosis 29 5.818
66
FRS001 Far Eastern Spotted Fever 24 5.818
67
LWG006 Low Grade Glioma 41 5.818
68
P YWS001 Yaws 36 5.818
69
c TRS027 Torsion Dystonia 4 19 5.818
70
P LPR021 Leprosy 3 71 5.818
71
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 5.818
72
CRR001 Carrion's Disease 31 5.818
73
SNN001 Sennetsu Fever 21 5.818
74
BCL011 Bacillary Angiomatosis 29 5.818
75
PRM026 Primary Systemic Mycosis 31 5.818
76
BSD001 Basidiobolomycosis 26 5.818
77
CMM006 Commensal Bacterial Infectious Disease 26 5.818
78
OPP001 Opportunistic Bacterial Infectious Disease 24 5.818
79
c PTT060 Pituitary Adenoma 5, Multiple Types 39 5.818
80
SPT006 Septooptic Dysplasia 62 5.818
81
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 5.818
82
MCS006 Macs Syndrome 57 5.818
83
CNJ002 Conjunctival Folliculosis 25 5.818
84
CTS002 Cat-Scratch Disease 42 5.818
85
c INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 26 5.818
86
P PRM030 Permanent Neonatal Diabetes Mellitus 59 5.818
87
END074 Endocardium Disease 24 5.818
88
CMP002 Campylobacteriosis 50 5.818
89
c CHR059 Chronic Endophthalmitis 22 5.818
90
CHN002 Chancroid 36 5.818
91
INC003 Inclusion Conjunctivitis 35 5.818
92
CRV030 Cervical Adenitis 34 5.818
93
BRT043 Bartonellosis 35 5.818
94
TST015 Testicular Disease 42 5.818
95
RLP003 Relapsing Fever 50 5.818
96
HVR001 Haverhill Fever 31 5.818
97
GLN002 Glanders 38 5.818
98
TRN004 Trench Fever 29 5.818
99
EHR002 Ehrlichiosis 39 5.818
100
P TCD001 Tic Disorder 50 5.818
101
TLR001 Tularemia 56 5.818
102
TCK004 Tick Infestation 29 5.818
103
MYC015 Mycobacterium Fortuitum 28 5.818
104
NCR004 Nocardiosis 52 5.818
105
MLT006 Multidrug-Resistant Tuberculosis 47 5.818
106
END016 Endocervicitis 31 5.818
107
TNS014 Tenosynovitis 45 5.818
108
MYC016 Mycobacterium Gordonae 20 5.818
109
LYM116 Lymph Node Disease 42 5.818
110
c ATS470 Autosomal Dominant Pure Spastic Paraplegia 14 5.818
111
c SPS021 Spastic Paraplegia 10 27 2.777
112
SQM006 Squamous Cell Carcinoma 59 1.744
113
P BRS047 Breast Cancer 97 1.593
114
ORL015 Oral Squamous Cell Carcinoma 43 1.491
115
P ATS364 Autism 72 1.446
116
ORL011 Oral Cancer 60 1.190
117
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 55 1.166
118
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 62 1.141
119
GLB002 Glioblastoma 67 1.141
120
P SPS012 Spastic Paraplegia 3a 32 1.141
121
c SPS036 Spastic Paraplegia 3 32 1.114
122
SPS057 Spasticity 43 1.114
123
c SPS091 Spastic Paraplegia 4 27 1.114
124
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.085
125
RNL077 Renal Fibrosis 46 1.085
126
IGG001 Iga Glomerulonephritis 50 1.085
127
URT010 Ureteral Obstruction 45 1.085
128
OST159 Osteogenic Sarcoma 66 1.054
129
P PLZ001 Pelizaeus-Merzbacher Disease 65 1.020
130
HYP066 Hyperglycemia 60 0.980
131
c MCR133 Microvascular Complications of Diabetes 4 41 0.934
132
c MCR113 Microvascular Complications of Diabetes 3 52 0.934
133
c MCR130 Microvascular Complications of Diabetes 6 41 0.934
134
c MCR120 Microvascular Complications of Diabetes 7 47 0.934
135
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.873
136
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.870
137
P KRT005 Keratoacanthoma 47 0.726
138
P PNC035 Pancreatic Cancer 86 0.573
139
c ATR087 Atrial Standstill 1 74 0.440
140
HYP060 Hyperinsulinism 53 0.388
141
P PRK057 Parkinson Disease, Late-Onset 79 0.293
142
AGN016 Aging 54 0.254
143
HMC014 Homocysteinemia 52 0.254
144
P HNT016 Huntington Disease 73 0.254
145
P CLR023 Colorectal Cancer 100 0.254
146
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.254
147
GST040 Gastric Adenocarcinoma 66 0.254
148
LNG099 Lung Disease 62 0.254
149
P PRS040 Prostate Cancer 95 0.207
150
c LKD015 Leukodystrophy, Hypomyelinating, 3 42 0.207
151
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.207
152
TBL029 Tubulin, Beta 28 0.207
153
CKT002 Cakut 48 0.207
154
c SML038 Small Cell Cancer of the Lung 69 0.207
155
c BRD014 Bardet-Biedl Syndrome 2 53 0.207
156
P HPT023 Hepatocellular Carcinoma 95 0.207
157
CLT003 Colitis 63 0.207
158
SVR001 Severe Acute Respiratory Syndrome 68 0.207
159
CYS009 Cystadenoma 43 0.207
160
BRN028 Brain Cancer 73 0.207
161
P PLM036 Pulmonary Fibrosis 65 0.207
162
P GLL018 Gallbladder Cancer 53 0.207
163
ADR007 Adrenoleukodystrophy 74 0.207
164
OVR094 Ovarian Epithelial Cancer 39 0.207
165
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.207
166
ADR022 Adrenomyeloneuropathy 39 0.207
167
ULC004 Ulcerative Colitis 74 0.207
168
ALL006 Allergic Asthma 56 0.207
169
MLG164 Malignant Epithelial Tumor of Ovary 24 0.207
170
P SCH015 Schizophrenia 74 0.147
171
PRS129 Prostatic Hyperplasia, Benign 48 0.147
172
HLC007 Helicobacter Pylori Infection 67 0.147
173
MYL069 Myeloma, Multiple 77 0.147
174
c BRD010 Bardet-Biedl Syndrome 1 64 0.147
175
c MCR115 Microvascular Complications of Diabetes 5 65 0.147
176
c SPS148 Spastic Paraplegia 31, Autosomal Dominant 48 0.147
177
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.147
178
c LKD019 Leukodystrophy, Hypomyelinating, 6 52 0.147
179
MNT001 Mantle Cell Lymphoma 65 0.147
180
P OPN001 Open-Angle Glaucoma 55 0.147
181
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.147
182
CRB004 Cerebral Artery Occlusion 46 0.147
183
BNS007 Bone Sarcoma 51 0.147
184
P LNG032 Lung Cancer 98 0.147
185
MST006 Mast Syndrome 40 0.147
186
SRN001 Serine Deficiency 23 0.147
187
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.147
188
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.147
189
c OPT053 Optic Atrophy 1 62 0.147
190
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.147
191
P LNG064 Lung Cancer Susceptibility 3 70 0.147
192
CHL065 Cholangiocarcinoma 58 0.147
193
c GLC092 Glaucoma, Primary Open Angle 61 0.147
194
P GLM040 Glioma Susceptibility 1 70 0.147
195
CHL068 Cholestasis 61 0.147
196
MLG169 Malignant Astrocytoma 57 0.147
197
PRS021 Prostatic Adenoma 43 0.147
198
c ACT027 Acute Pancreatitis 60 0.147
199
P ADN016 Adenocarcinoma 63 0.147
200
ADN018 Adenoma 58 0.147
201
SPN051 Spondylitis 51 0.147
202
INT079 Intrahepatic Cholangiocarcinoma 51 0.147
203
P PNC044 Pancreatitis 61 0.147
204
PRS045 Prostatic Hypertrophy 52 0.147
205
P MLN008 Melanoma 75 0.147
206
P BRD002 Bardet-Biedl Syndrome 66 0.147
207
MNT002 Mental Depression 56 0.147
208
KLB003 Klebsiella Pneumonia 49 0.147
209
P HYP069 Hyperparathyroidism 62 0.147
210
P HYP061 Hypertrophic Cardiomyopathy 69 0.147
211
INF009 Inflammatory Spondylopathy 30 0.147
212
ALL029 Allergic Disease 61 0.147
213
SLC006 Silicosis 55 0.147
214
c SCN007 Secondary Hyperparathyroidism 51 0.147
215
CLN015 Colon Adenocarcinoma 64 0.147
216
EMB004 Embryonal Carcinoma 55 0.147
217
c SPS127 Spastic Paraplegia 6, Autosomal Dominant 48 0.147
218
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 52 0.147
219
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.147
220
ANR007 Anorexia Nervosa 59 0.147
221
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.147
222
P MSC003 Muscular Atrophy 52 0.147
223
XLN085 X-Linked Complicated Spastic Paraplegia Type 1 21 0.147
224
HYP266 Hypoxia 56 0.147
225
48X005 48,xyyy 39 0.147
226
c SPS041 Spastic Paraplegia 6 26 0.147
227
PRT036 Peritonitis 65 0.147
228
CHC001 Chickenpox 56 0.147
229
c SPS013 Spastic Paraplegia 8 30 0.147
230
P CHL066 Cholangitis 51 0.147
231
ETN001 Eating Disorder 59 0.147
232
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.147
233
P PRH002 Pure Hereditary Spastic Paraplegia 21 0.147
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