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

166 hits were found for 'exostoses'

# ++ Fam MCID Name MIFTS Score
1
HRD001 Hereditary Multiple Exostoses 47 8.498
2
P EXS004 Exostoses, Multiple, Type 1 29 4.483
3
HRD104 Hereditary Multiple Osteochondromas 27 4.421
4
EXS003 Exostoses Anetodermia Brachydactyly Type E 8 4.305
5
c EXS006 Exostoses, Multiple, Type 3 7 4.283
6
SPS051 Spasticity Multiple Exostoses 2 3.777
7
c EXS005 Exostoses, Multiple, Type 2 5 3.757
8
CRN096 Craniosynostosis Exostoses Nevus Epibulbar Dermoid 0 3.058
9
EXS001 Exostosis 49 2.490
10
DPY002 Dupuytren Subungual Exostosis 4 2.141
11
OST028 Osteochondroma 49 0.279
12
P CNG124 Congenital Rubella 51 0.227
13
IDP042 Idiopathic Recurrent Stupor 15 0.177
14
SCN006 Secondary Syphilis 53 0.164
15
MTC018 Metachondromatosis 27 0.164
16
ANK002 Ankylosing Spondylitis 75 0.157
17
c BRC013 Brachydactyly Type E 36 0.157
18
P CHN012 Chondrosarcoma 50 0.149
19
ACT131 Acetabular Dysplasia 17 0.149
20
MNN014 Mononeuritis 40 0.142
21
P TRC085 Trichorhinophalangeal Syndrome Type Ii 40 0.142
22
ATX002 Ataxia Telangiectasia 81 0.134
23
NTR003 Natural Killer Cell Leukemia 52 0.134
24
c MNT147 Mental Retardation 51 0.134
25
GLL008 Gilles De La Tourette Syndrome 60 0.125
26
ACT019 Acute Myeloid Leukemia 87 0.116
27
ACN002 Acanthosis Nigricans 70 0.116
28
OCC006 Occipital Horn Syndrome 57 0.116
29
THR013 Thoracic Outlet Syndrome 53 0.116
30
GLM037 Glioma Somatic 27 0.116
31
GRF006 Grfoma 20 0.116
32
PRL042 Proliferating Trichilemmal Cyst 40 0.106
33
HNM001 Hinman's Syndrome 28 0.106
34
P SHR002 Short Stature 64 0.094
35
c BRC006 Brachydactyly 48 0.094
36
PTC001 Potocki-Shaffer Syndrome 35 0.094
37
DYS048 Dysplasia Epiphysealis Hemimelica 34 0.094
38
SHL001 Shoulder Impingement Syndrome 20 0.094
39
KLD003 Keloid Formation 19 0.094
40
P OST012 Osteoarthritis 72 0.082
41
LKM002 Leukemia 70 0.082
42
P SCH015 Schizophrenia 69 0.082
43
WST001 West Syndrome 64 0.082
44
P SYN007 Synovitis 58 0.082
45
NRP001 Neuropathy 54 0.082
46
PSR002 Psoriasis 51 0.082
47
ANK001 Ankylosis 51 0.082
48
PRC013 Pericarditis 48 0.082
49
PRC012 Pericardial Effusion 47 0.082
50
DYS073 Dysphagia 42 0.082
51
P CRV039 Cervicitis 41 0.082
52
CHL079 Children's Interstitial Lung Disease 39 0.082
53
c ATX010 Ataxia Neuropathy Spectrum 33 0.082
54
JVN024 Juvenile Hereditary Hemochromatosis 28 0.082
55
LRW003 L�ri-Weill Dyschondrosteosis 25 0.082
56
c GLM039 Glomerulosclerosis, Focal Segmental, 6 24 0.082
57
c TTL001 Total Internal Ophthalmoplegia 17 0.082
58
AND002 Androgen Insensitivity Syndrome 75 0.067
59
P OST018 Osteosarcoma 70 0.067
60
P AST007 Astrocytoma 70 0.067
61
HPT023 Hepatocellular Carcinoma 69 0.067
62
P ANG001 Angelman Syndrome 67 0.067
63
CLN016 Colon Cancer 66 0.067
64
RLP001 Relapsing Polychondritis 66 0.067
65
ART019 Aortic Valve Stenosis 64 0.067
66
MYL006 Myeloid Leukemia 64 0.067
67
c CRN037 Craniosynostosis 62 0.067
68
OLL001 Ollier Disease 62 0.067
69
P ADN016 Adenocarcinoma 60 0.067
70
ALB001 Albright's Hereditary Osteodystrophy 59 0.067
71
SPN051 Spondylitis 59 0.067
72
NSY001 N Syndrome 57 0.067
73
c AXN002 Axenfeld-Rieger Syndrome 57 0.067
74
MYC002 Mycobacterium Avium Complex Disease 56 0.067
75
P SHR029 Short Syndrome 55 0.067
76
P PRT008 Proteus Syndrome 55 0.067
77
SPN027 Spinal Stenosis 53 0.067
78
SPN020 Spondylosis 53 0.067
79
KLD001 Keloids 52 0.067
80
ART001 Arterial Tortuosity Syndrome 52 0.067
81
P PND001 Pain Disorder 49 0.067
82
c PSD015 Pseudohypoparathyroidism 49 0.067
83
LNN001 Lennox-Gastaut Syndrome 46 0.067
84
P BRS044 Breast Adenocarcinoma 45 0.067
85
MLK003 Melkersson-Rosenthal Syndrome 43 0.067
86
SPS057 Spasticity 42 0.067
87
ATX019 Ataxia with Vitamin E Deficiency 40 0.067
88
AND003 Andersen-Tawil Syndrome 39 0.067
89
BNC001 Bone Carcinoma 39 0.067
90
CRY008 Cryopyrin-Associated Periodic Syndrome 35 0.067
91
HMN001 Human Monocytic Ehrlichiosis 33 0.067
92
c TRC004 Trichorhinophalangeal Syndrome Type I 32 0.067
93
CRB026 Cerebellar Astrocytoma 26 0.067
94
FMR003 Femoral Neuropathy 25 0.067
95
c BRC038 Brachydactyly Type B 24 0.067
96
c BNG076 Benign Exophthalmos Syndrome 17 0.067
97
P RHM011 Rheumatoid Arthritis 83 0.047
98
P LFR001 Li-Fraumeni Syndrome 75 0.047
99
P ART022 Arthritis 75 0.047
100
ATS001 Autistic Disorder 71 0.047
101
MNK001 Menkes Disease 71 0.047
102
GLN003 Glanzmann's Thrombasthenia 68 0.047
103
FBR011 Fibrodysplasia Ossificans Progressiva 66 0.047
104
ACT073 Acute Leukemia 62 0.047
105
HYP042 Hypochondroplasia 62 0.047
106
P DWR001 Dwarfism 59 0.047
107
CRY002 Cryptorchidism 59 0.047
108
P CTS001 Cutis Laxa 59 0.047
109
NLP001 Nail-Patella Syndrome 58 0.047
110
ANR008 Aneurysm Disease 57 0.047
111
INT051 Intussusception 57 0.047
112
GYN001 Gynecomastia 56 0.047
113
FBR003 Fibrous Histiocytoma 54 0.047
114
HYP017 Hypophosphatemia 52 0.047
115
P SPN052 Spondyloarthropathy 52 0.047
116
c SYN005 Synostosis 51 0.047
117
DRM004 Dermatofibrosarcoma 51 0.047
118
OST014 Osteopoikilosis 50 0.047
119
WGR001 Wagr Syndrome 50 0.047
120
OST003 Osteonecrosis 49 0.047
121
HST009 Histiocytoma 49 0.047
122
CLC006 Calcinosis 49 0.047
123
HMP005 Hemiplegia 47 0.047
124
SKL017 Skeletal Dysplasias 47 0.047
125
P DNT009 Dentin Dysplasia 46 0.047
126
P CWD006 Cowden Syndrome 1 46 0.047
127
DYS018 Dysostosis 45 0.047
128
c FTL001 Fetal Alcohol Syndrome 44 0.047
129
ANR009 Aneurysmal Bone Cysts 43 0.047
130
HYP077 Hypertrichosis 43 0.047
131
RCR001 Recurrent Corneal Erosion 43 0.047
132
P OTS001 Otosclerosis 41 0.047
133
INT052 Intestinal Volvulus 40 0.047
134
INC001 Incontinentia Pigmenti Achromians 39 0.047
135
PRT093 Proteus Syndrome, Somatic 39 0.047
136
ENC014 Enchondroma 38 0.047
137
P HRD086 Hereditary Hypophosphatemic Rickets 38 0.047
138
PRL008 Paralytic Ileus 37 0.047
139
PSD014 Pseudopseudohypoparathyroidism 37 0.047
140
c CRN035 Cranial Nerve Palsy 35 0.047
141
c BRC039 Brachydactyly Type C 33 0.047
142
MTR001 Mature Cataract 32 0.047
143
ADS002 Adie Syndrome 32 0.047
144
TTH001 Tooth Ankylosis 31 0.047
145
LRW002 Leri Weill Dyschondrosteosis 27 0.047
146
OCL034 Oculocerebrocutaneous Syndrome 27 0.047
147
c ENL009 Enlarged Parietal Foramina 25 0.047
148
c STC007 Stickler Syndrome, Type 3 23 0.047
149
BZX002 Bazex-Dupre-Christol Syndrome 22 0.047
150
AND005 Androgen Insensitivity Syndrome, Mild 19 0.047
151
c BRC050 Brachydactyly Type D 19 0.047
152
c SPN253 Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1, with or Without Fractures 19 0.047
153
HYP299 Hyperostosis, Endosteal 18 0.047
154
LTH004 Lathyrism 17 0.047
155
c 8P2001 8p23.1 Microduplication Syndrome 15 0.047
156
UPN001 Upington Disease 15 0.047
157
c CTR006 Cataract Anterior Polar Dominant 14 0.047
158
c ACT066 Acute Cervicitis 13 0.047
159
OTP003 Oto-Palatal-Digital Syndrome 13 0.047
160
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 13 0.047
161
BRC027 Brachydactyly Mononen Type 12 0.047
162
TWS001 Twist1-Related Craniosynostosis 12 0.047
163
MCR070 Microcornea, Glaucoma, and Absent Frontal Sinuses 11 0.047
164
DYS134 Dysspondyloenchondromatosis 10 0.047
165
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 8 0.047
166
c CHR267 Chromosome 8q Deletion 6 0.047