Search results for "exostoses"

The MalaCard for "exostoses" has been retired.
Searching MalaCards for entries containing "exostoses"

205 hits were found for 'exostoses'

# Family MCID Name MIFTS Score
1
P HRD001 Hereditary Multiple Exostoses 53 9.162
2
c HRD104 Hereditary Multiple Osteochondromas 28 5.525
3
c EXS004 Exostoses, Multiple, Type 1 26 4.776
4
c EXS005 Exostoses, Multiple, Type 2 23 4.254
5
EXS001 Exostosis 39 3.847
6
SPS051 Spasticity Multiple Exostoses 5 3.643
7
EXS003 Exostoses Anetodermia Brachydactyly Type E 12 2.992
8
c EXS006 Exostoses, Multiple, Type 3 10 2.956
9
OLL001 Ollier Disease 52 2.167
10
CRN096 Craniosynostosis Exostoses Nevus Epibulbar Dermoid 1 2.127
11
P HRD071 Hereditary Multiple Osteochondromatosis, Type I 8 2.103
12
c HRD072 Hereditary Multiple Osteochondromatosis, Type Ii 8 2.103
13
DPY002 Dupuytren Subungual Exostosis 2 2.039
14
P OST028 Osteochondroma 40 0.235
15
P CRV039 Cervicitis 42 0.193
16
P CHN012 Chondrosarcoma 52 0.160
17
P TRC091 Trichorhinophalangeal Syndrome, Type Ii 48 0.160
18
PTC001 Potocki-Shaffer Syndrome 39 0.147
19
c SCN006 Secondary Syphilis 48 0.125
20
P HRM001 Hermansky-Pudlak Syndrome 62 0.109
21
c PNC108 Pancreatitis, Hereditary 59 0.109
22
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.109
23
HNT002 Hantavirus Pulmonary Syndrome 52 0.109
24
MTC018 Metachondromatosis 32 0.109
25
LRW001 Leri-Weill Dyschondrosteosis 45 0.099
26
SKL017 Skeletal Dysplasias 39 0.099
27
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.089
28
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.089
29
ANR002 Aniridia 72 0.089
30
ACN002 Acanthosis Nigricans 53 0.089
31
OCC006 Occipital Horn Syndrome 50 0.089
32
P SHR029 Short Syndrome 49 0.089
33
P BRC006 Brachydactyly 48 0.089
34
THR013 Thoracic Outlet Syndrome 47 0.089
35
OST015 Osteochondrodysplasia 46 0.089
36
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.089
37
MRC001 Marchiafava Bignami Disease 42 0.089
38
SKL014 Skeletal Dysplasia 38 0.089
39
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.089
40
P ATX010 Ataxia Neuropathy Spectrum 31 0.089
41
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.089
42
c MLT019 Multiple Myeloma 77 0.077
43
P ATX030 Ataxia-Telangiectasia 76 0.077
44
c LKM061 Leukemia, Acute Myeloid 74 0.077
45
MYL009 Myelodysplastic Syndrome 69 0.077
46
BRK010 Burkitt Lymphoma 68 0.077
47
c SPN225 Spondyloarthropathy 1 66 0.077
48
P ANG001 Angelman Syndrome 66 0.077
49
AND015 Androgen Insensitivity 65 0.077
50
P LKM002 Leukemia 61 0.077
51
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.077
52
ART001 Arterial Tortuosity Syndrome 59 0.077
53
c MCP004 Mucopolysaccharidosis Iv 58 0.077
54
P AND016 Andersen Syndrome 58 0.077
55
OST085 Osteosarcoma, Somatic 56 0.077
56
P MYL007 Myeloma 54 0.077
57
CHL071 Child Syndrome 51 0.077
58
MLL005 Miller-Dieker Syndrome 50 0.077
59
BNC003 Bone Cancer 50 0.077
60
CNN005 Connective Tissue Disease 49 0.077
61
P NRP001 Neuropathy 48 0.077
62
c ART101 Aortic Valve Disease 2 46 0.077
63
c MCP038 Mucopolysaccharidosis Iva 46 0.077
64
P MST018 Mesothelioma 45 0.077
65
P CTN015 Cutaneous T Cell Lymphoma 45 0.077
66
HYP068 Hyperostosis 45 0.077
67
KDS001 Kid Syndrome 44 0.077
68
c MLG079 Malignant Pleural Mesothelioma 43 0.077
69
ANR040 Aneurysm 43 0.077
70
P TRC086 Trichohepatoenteric Syndrome 1 42 0.077
71
SPN051 Spondylitis 39 0.077
72
MNN014 Mononeuritis 39 0.077
73
c BNG032 Benign Mesothelioma 32 0.077
74
P CNN004 Connective Tissue Cancer 31 0.077
75
SPS057 Spasticity 30 0.077
76
BND014 Bone Development Disease 28 0.077
77
c CNN010 Connective Tissue Benign Neoplasm 28 0.077
78
TFT003 Tufting Enteropathy 27 0.077
79
c ACT219 Acute Myeloid Leukemia, Flt3-Related 23 0.077
80
ALR002 Al-Raqad Syndrome 23 0.077
81
MDL024 Madelung Deformity 23 0.077
82
FML045 Familial Mosaic Monosomy 7 Syndrome 17 0.077
83
P BRS047 Breast Cancer 100 0.063
84
P SCH015 Schizophrenia 79 0.063
85
MNK001 Menkes Disease 65 0.063
86
P PSR002 Psoriasis 64 0.063
87
P MYL006 Myeloid Leukemia 59 0.063
88
NLP001 Nail-Patella Syndrome 59 0.063
89
P LYM026 Lymphoblastic Leukemia 57 0.063
90
P ATP001 Atopic Dermatitis 57 0.063
91
P CRN037 Craniosynostosis 57 0.063
92
DRM006 Dermatitis 54 0.063
93
PRT093 Proteus Syndrome, Somatic 52 0.063
94
PLM129 Pulmonary Disease, Chronic Obstructive 51 0.063
95
MFF001 Maffucci Syndrome 47 0.063
96
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.063
97
c TRC092 Trichorhinophalangeal Syndrome, Type I 43 0.063
98
P PSD015 Pseudohypoparathyroidism 42 0.063
99
PRC012 Pericardial Effusion 41 0.063
100
HMM002 Haim-Munk Syndrome 40 0.063
101
MNT002 Mental Depression 39 0.063
102
GRW007 Growth Hormone Deficiency 38 0.063
103
BZX001 Bazex Syndrome 37 0.063
104
DYS073 Dysphagia 33 0.063
105
DYS048 Dysplasia Epiphysealis Hemimelica 33 0.063
106
c STC014 Stickler Syndrome, Type Iii 32 0.063
107
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.063
108
OCL034 Oculocerebrocutaneous Syndrome 30 0.063
109
FMR003 Femoral Neuropathy 30 0.063
110
HMN001 Human Monocytic Ehrlichiosis 29 0.063
111
c ACT066 Acute Cervicitis 29 0.063
112
LWC001 Low Compliance Bladder 28 0.063
113
c BNG076 Benign Exophthalmos Syndrome 21 0.063
114
DYS134 Dysspondyloenchondromatosis 19 0.063
115
UPN001 Upington Disease 17 0.063
116
BRC027 Brachydactyly Mononen Type 16 0.063
117
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 15 0.063
118
8P2001 8p23.1 Microduplication Syndrome 12 0.063
119
c FML303 Familial/multiple Cancer 6 0.063
120
P CLR023 Colorectal Cancer 95 0.044
121
P RHM011 Rheumatoid Arthritis 88 0.044
122
P OST012 Osteoarthritis 79 0.044
123
GLL008 Gilles De La Tourette Syndrome 67 0.044
124
GLN010 Glanzmann Thrombasthenia 65 0.044
125
c LKM062 Leukemia, Acute Lymphoblastic 63 0.044
126
ATS001 Autistic Disorder 62 0.044
127
P ART022 Arthritis 61 0.044
128
FBR011 Fibrodysplasia Ossificans Progressiva 60 0.044
129
ELL001 Ellis-Van Creveld Syndrome 57 0.044
130
P ADN016 Adenocarcinoma 56 0.044
131
HYP042 Hypochondroplasia 56 0.044
132
IMG001 Image Syndrome 56 0.044
133
P AST007 Astrocytoma 55 0.044
134
SPN186 Spinal Cord Injury 55 0.044
135
VSC007 Vascular Disease 55 0.044
136
WGR001 Wagr Syndrome 55 0.044
137
P MLT007 Multiple Epiphyseal Dysplasia 53 0.044
138
MLK003 Melkersson-Rosenthal Syndrome 53 0.044
139
CRY002 Cryptorchidism 52 0.044
140
P CTS001 Cutis Laxa 51 0.044
141
P FTL001 Fetal Alcohol Syndrome 50 0.044
142
OST003 Osteonecrosis 50 0.044
143
PSD014 Pseudopseudohypoparathyroidism 50 0.044
144
P HYP613 Hypophosphatemic Rickets 49 0.044
145
P ACT074 Acute Lymphocytic Leukemia 48 0.044
146
HYP299 Hyperostosis, Endosteal 46 0.044
147
SPN027 Spinal Stenosis 46 0.044
148
SPN020 Spondylosis 46 0.044
149
MYC002 Mycobacterium Avium Complex Disease 46 0.044
150
c BRC082 Brachydactyly, Type E 44 0.044
151
LNN001 Lennox-Gastaut Syndrome 44 0.044
152
SYN007 Synovitis 44 0.044
153
P SCL018 Scoliosis 44 0.044
154
PRC013 Pericarditis 44 0.044
155
P OTS001 Otosclerosis 43 0.044
156
P BRS044 Breast Adenocarcinoma 43 0.044
157
c PND001 Pain Disorder 43 0.044
158
INC001 Incontinentia Pigmenti Achromians 43 0.044
159
ADL002 Adult Syndrome 43 0.044
160
HMP005 Hemiplegia 43 0.044
161
DYS018 Dysostosis 43 0.044
162
ANK001 Ankylosis 43 0.044
163
DWR001 Dwarfism 42 0.044
164
CLC006 Calcinosis 42 0.044
165
KLD001 Keloids 42 0.044
166
SYN005 Synostosis 41 0.044
167
HYP077 Hypertrichosis 40 0.044
168
c CWD006 Cowden Syndrome 1 39 0.044
169
GYN001 Gynecomastia 39 0.044
170
HYP017 Hypophosphatemia 39 0.044
171
CRP017 Carpal Tunnel Syndrome, Familial 39 0.044
172
TTH001 Tooth Ankylosis 38 0.044
173
P CHN059 Chondrocalcinosis 38 0.044
174
HST009 Histiocytoma 38 0.044
175
NTR003 Natural Killer Cell Leukemia 38 0.044
176
FBR003 Fibrous Histiocytoma 37 0.044
177
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 36 0.044
178
RGH009 Right Atrial Isomerism 36 0.044
179
SHL001 Shoulder Impingement Syndrome 35 0.044
180
P DNT009 Dentin Dysplasia 35 0.044
181
c HRD086 Hereditary Hypophosphatemic Rickets 34 0.044
182
ADS002 Adie Syndrome 34 0.044
183
P CRN035 Cranial Nerve Palsy 33 0.044
184
HMP001 Hemopericardium 33 0.044
185
HPT074 Hepatic Adenoma, Somatic 30 0.044
186
PST011 Pustulosis of Palm and Sole 28 0.044
187
c PSR017 Psoriasis 2 28 0.044
188
P PSR004 Psoriasis Susceptibility 1 28 0.044
189
SPN253 Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1, with or Without Fractures 28 0.044
190
HNM002 Hinman Syndrome 27 0.044
191
CRB026 Cerebellar Astrocytoma 26 0.044
192
P PRT063 Proteus-Like Syndrome 26 0.044
193
SPC003 Specific Developmental Disorder 25 0.044
194
c CRN215 Cornelia De Lange Syndrome 4 24 0.044
195
KLD003 Keloid Formation 24 0.044
196
c PSR019 Psoriasis Susceptibility 13 23 0.044
197
P SPN127 Spondyloepimetaphyseal Dysplasia Joint Laxity 21 0.044
198
PSR005 Psoriasis, Protection Against 21 0.044
199
HLS001 Heel Spur 20 0.044
200
AND005 Androgen Insensitivity Syndrome, Mild 19 0.044
201
OST076 Osteochondritis Dissecans, Short Stature, and Early-Onset Osteoarthritis 18 0.044
202
LTH004 Lathyrism 17 0.044
203
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 15 0.044
204
MCR070 Microcornea, Glaucoma, and Absent Frontal Sinuses 13 0.044
205
DVL012 Developmental Dysplasia of the Hip 1 13 0.044