Search results for Dermatan

148 hits were found for Dermatan

# Family MCID Name MIFTS Score
1
c EHL076 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1 34 2.785
2
EHL015 Ehlers-Danlos Syndrome Progeroid Type 45 2.745
3
P EHL001 Ehlers-Danlos Syndrome 58 0.199
4
c THR092 Thrombophilia Due to Thrombin Defect 73 0.174
5
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.174
6
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.153
7
MCP033 Mucopolysaccharidoses 38 0.153
8
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.145
9
SCH036 Scheie Syndrome 72 0.137
10
CLB002 Clubfoot 51 0.137
11
P MSC134 Musculocontractural Ehlers-Danlos Syndrome 40 0.137
12
P THR014 Thrombocytopenia 67 0.118
13
PLM033 Pulmonary Embolism 59 0.118
14
HPR003 Heparin-Induced Thrombocytopenia 48 0.118
15
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.118
16
HRL003 Hurler Syndrome 65 0.108
17
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.108
18
P VSC007 Vascular Disease 63 0.097
19
HRL004 Hurler-Scheie Syndrome 55 0.097
20
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 41 0.097
21
P KDN018 Kidney Disease 72 0.084
22
CNN005 Connective Tissue Disease 68 0.084
23
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.084
24
OST159 Osteogenic Sarcoma 66 0.084
25
P PLM036 Pulmonary Fibrosis 65 0.084
26
P BPL003 Bipolar Disorder 56 0.084
27
P CHN012 Chondrosarcoma 56 0.084
28
MCS002 Mucositis 56 0.084
29
URT010 Ureteral Obstruction 45 0.084
30
c MJR024 Major Affective Disorder 9 41 0.084
31
HPR006 Heparin Cofactor Ii Deficiency 40 0.084
32
c MJR022 Major Affective Disorder 8 38 0.084
33
P BRS047 Breast Cancer 97 0.068
34
OST012 Osteoarthritis 78 0.068
35
LVR012 Liver Cirrhosis 62 0.068
36
DSS009 Disseminated Intravascular Coagulation 57 0.068
37
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.068
38
THR024 Thrombosis 57 0.068
39
c MCR113 Microvascular Complications of Diabetes 3 52 0.068
40
47X002 47,xyy 49 0.068
41
HLX001 Helix Syndrome 47 0.068
42
c MCR120 Microvascular Complications of Diabetes 7 47 0.068
44
FBR054 Fibroma 44 0.068
45
MLT162 Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects 42 0.068
46
c MCR130 Microvascular Complications of Diabetes 6 41 0.068
47
c MCR133 Microvascular Complications of Diabetes 4 41 0.068
48
EXN003 Exencephaly 31 0.068
49
CNG065 Congenital Contractures 27 0.068
50
c EHL086 Ehlers-Danlos Syndrome, Musculocontractural Type, 2 25 0.068
51
OVR098 Ovarian Fibroma 25 0.068
52
P CLR023 Colorectal Cancer 99 0.048
53
P OVR042 Ovarian Cancer 88 0.048
54
P ALZ034 Alzheimer Disease 88 0.048
55
NRL016 Neural Tube Defects 82 0.048
56
CYS001 Cystic Fibrosis 81 0.048
57
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.048
58
INS024 Insulin-Like Growth Factor I 79 0.048
59
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.048
60
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.048
61
c ATR087 Atrial Standstill 1 75 0.048
62
c HYP836 Hypercholesterolemia, Familial, 1 73 0.048
63
MSC157 Muscular Dystrophy, Duchenne Type 72 0.048
64
P AMY004 Amyloidosis 70 0.048
65
P MLN008 Melanoma 69 0.048
66
ART016 Aortic Aneurysm 69 0.048
67
P LKM062 Leukemia, Acute Lymphoblastic 69 0.048
68
P LYM118 Lymphoma 68 0.048
69
P LVR013 Liver Disease 68 0.048
70
RCK004 Rickets 68 0.048
71
PNC129 Pancreatic Adenocarcinoma 68 0.048
72
P MSC005 Muscular Dystrophy 66 0.048
73
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.048
74
P PSD087 Pseudoxanthoma Elasticum 65 0.048
75
AFB002 Afibrinogenemia, Congenital 65 0.048
76
ATH013 Atherosclerosis Susceptibility 65 0.048
77
PRT036 Peritonitis 64 0.048
78
NRM005 Neuromuscular Disease 64 0.048
79
P ADN016 Adenocarcinoma 64 0.048
80
LYM017 Lyme Disease 64 0.048
81
c PRC016 Pre-Eclampsia 63 0.048
82
LPD008 Lipid Metabolism Disorder 62 0.048
83
P PSR002 Psoriasis 62 0.048
84
c HPT003 Hepatitis a 62 0.048
85
c SVR001 Severe Acute Respiratory Syndrome 62 0.048
86
P LRS001 Larsen Syndrome 62 0.048
87
ATM095 Autoimmune Disease 62 0.048
88
HYP066 Hyperglycemia 61 0.048
89
c SCL052 Scleroderma, Familial Progressive 61 0.048
90
RCT015 Reactive Arthritis 61 0.048
91
SPN186 Spinal Cord Injury 60 0.048
92
P SCL018 Scoliosis 60 0.048
93
SQM006 Squamous Cell Carcinoma 60 0.048
94
ING001 Inguinal Hernia 60 0.048
95
c ACT071 Acute Kidney Failure 60 0.048
96
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.048
97
ANR040 Aneurysm 59 0.048
98
c ACT073 Acute Leukemia 58 0.048
99
c ACT075 Acute Myocardial Infarction 57 0.048
100
P FCL005 Focal Segmental Glomerulosclerosis 57 0.048
101
EMB004 Embryonal Carcinoma 56 0.048
102
P LRY044 Larynx Cancer 55 0.048
103
MCL075 Macular Dystrophy, Corneal 54 0.048
104
P INF037 Inflammatory Bowel Disease 54 0.048
105
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.048
106
c EXS019 Exostoses, Multiple, Type I 53 0.048
107
HMC014 Homocysteinemia 53 0.048
108
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.048
109
LYS002 Lysosomal Storage Disease 52 0.048
110
PST011 Pustulosis of Palm and Sole 52 0.048
111
ART074 Aortic Dissection 52 0.048
112
P PST095 Post-Thrombotic Syndrome 51 0.048
113
TMT002 Temtamy Preaxial Brachydactyly Syndrome 50 0.048
114
P ECL001 Eclampsia 50 0.048
115
CRN030 Coronary Stenosis 50 0.048
116
c SVR005 Severe Pre-Eclampsia 50 0.048
117
HYP748 Hypertelorism 50 0.048
118
NPH010 Nephrosclerosis 50 0.048
119
P CRN025 Corneal Dystrophy 49 0.048
120
c DSB006 Desbuquois Dysplasia 1 48 0.048
121
ATS010 Autosomal Recessive Disease 48 0.048
122
c CRN241 Corneal Dystrophy, Congenital Stromal 48 0.048
123
RNL077 Renal Fibrosis 47 0.048
124
UMB002 Umbilical Hernia 46 0.048
125
ESP027 Esophagus Squamous Cell Carcinoma 45 0.048
126
CRT015 Carotid Artery Occlusion 45 0.048
127
c PCH010 Pachyonychia Congenita 3 44 0.048
128
DWR001 Dwarfism 44 0.048
129
PRT011 Protein C Deficiency 44 0.048
130
DYS018 Dysostosis 44 0.048
131
RFR003 Refractive Error 43 0.048
132
FBR019 Fibromatosis 41 0.048
133
ALL014 Allergic Encephalomyelitis 38 0.048
134
CRT004 Carotid Artery Thrombosis 38 0.048
135
SPN331 Spondyloocular Syndrome 36 0.048
136
ABD010 Abdominal Wall Defect 36 0.048
137
HRW001 Hair Whorl 36 0.048
138
MST021 Meester-Loeys Syndrome 35 0.048
139
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.048
140
P DSB002 Desbuquois Dysplasia 32 0.048
141
P SPN127 Spondyloepimetaphyseal Dysplasia Joint Laxity 31 0.048
142
MCL022 Mucolipidoses 30 0.048
143
P PRG139 Progeroid Syndrome 28 0.048
144
ARG004 Argyria 27 0.048
145
STR086 Stromal Dystrophy 26 0.048
146
CRN273 Corneal Dystrophy, Subepithelial Mucinous 25 0.048
147
LYS030 Lysosomal Storage Disease with Skeletal Involvement 25 0.048
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