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

159 hits were found for 'exostoses'

# Family MCID Name MIFTS Score
1
HRD001 Hereditary Multiple Exostoses 50 8.513
2
HRD104 Hereditary Multiple Osteochondromas 32 4.589
3
P EXS004 Exostoses, Multiple, Type 1 40 4.509
4
EXS003 Exostoses Anetodermia Brachydactyly Type E 13 4.305
5
c EXS006 Exostoses, Multiple, Type 3 7 4.283
6
SPS051 Spasticity Multiple Exostoses 2 3.778
7
c EXS005 Exostoses, Multiple, Type 2 11 3.757
8
CRN096 Craniosynostosis Exostoses Nevus Epibulbar Dermoid 0 3.059
9
EXS001 Exostosis 54 2.495
10
DPY002 Dupuytren Subungual Exostosis 1 2.141
11
c CNG124 Congenital Rubella 42 0.230
12
P CRV039 Cervicitis 52 0.197
13
SCN006 Secondary Syphilis 55 0.192
14
OST028 Osteochondroma 37 0.192
15
IDP042 Idiopathic Recurrent Stupor 15 0.179
16
MTC018 Metachondromatosis 26 0.166
17
ANK002 Ankylosing Spondylitis 75 0.159
18
P CHN012 Chondrosarcoma 63 0.151
19
MNN014 Mononeuritis 48 0.144
20
P TRC085 Trichorhinophalangeal Syndrome Type Ii 47 0.144
21
c BRC013 Brachydactyly Type E 38 0.144
22
ACT131 Acetabular Dysplasia 10 0.144
23
P ATX002 Ataxia Telangiectasia 93 0.135
24
NTR003 Natural Killer Cell Leukemia 56 0.135
25
GLL008 Gilles De La Tourette Syndrome 73 0.127
26
P ACT019 Acute Myeloid Leukemia 94 0.117
27
ACN002 Acanthosis Nigricans 73 0.117
28
OCC006 Occipital Horn Syndrome 57 0.117
29
THR013 Thoracic Outlet Syndrome 54 0.117
30
GLM037 Glioma Somatic 31 0.117
31
GRF006 Grfoma 26 0.117
32
GRW022 Growth Retardation-Mild Developmental Delay-Chronic Hepatitis Syndrome 18 0.117
33
PRL042 Proliferating Trichilemmal Cyst 38 0.107
34
c BRC006 Brachydactyly 48 0.096
35
LRW002 Leri Weill Dyschondrosteosis 42 0.096
36
DYS048 Dysplasia Epiphysealis Hemimelica 31 0.096
37
HNM002 Hinman Syndrome 24 0.096
38
SHL001 Shoulder Impingement Syndrome 21 0.096
39
P LKM002 Leukemia 79 0.083
40
P SCH015 Schizophrenia 77 0.083
41
P OST012 Osteoarthritis 73 0.083
42
WST001 West Syndrome 64 0.083
43
NRP001 Neuropathy 61 0.083
44
PSR002 Psoriasis 60 0.083
45
PRC013 Pericarditis 57 0.083
46
PRC012 Pericardial Effusion 54 0.083
47
ANK001 Ankylosis 50 0.083
48
CHL079 Children's Interstitial Lung Disease 46 0.083
49
P ATX010 Ataxia Neuropathy Spectrum 44 0.083
50
SYN053 Syndromic Diarrhea 42 0.083
51
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.083
52
PTC001 Potocki-Shaffer Syndrome 34 0.083
53
c GLM039 Glomerulosclerosis, Focal Segmental, 6 28 0.083
54
c TTL001 Total Internal Ophthalmoplegia 17 0.083
55
KLD003 Keloid Formation 16 0.083
56
HPT023 Hepatocellular Carcinoma 89 0.068
57
AND002 Androgen Insensitivity Syndrome 88 0.068
58
P OST018 Osteosarcoma 81 0.068
59
ALB001 Albright's Hereditary Osteodystrophy 74 0.068
60
c MYL006 Myeloid Leukemia 72 0.068
61
P AST007 Astrocytoma 72 0.068
62
OLL001 Ollier Disease 70 0.068
63
P ANG001 Angelman Syndrome 70 0.068
64
RLP001 Relapsing Polychondritis 69 0.068
65
ART019 Aortic Valve Stenosis 68 0.068
66
P CLN016 Colon Cancer 67 0.068
67
c CRN037 Craniosynostosis 67 0.068
68
ART001 Arterial Tortuosity Syndrome 62 0.068
69
SPN051 Spondylitis 60 0.068
70
c AXN002 Axenfeld-Rieger Syndrome 60 0.068
71
P ADN016 Adenocarcinoma 60 0.068
72
P SYN007 Synovitis 59 0.068
73
MYC002 Mycobacterium Avium Complex Disease 57 0.068
74
P PRT008 Proteus Syndrome 56 0.068
75
c PSD015 Pseudohypoparathyroidism 55 0.068
76
ATX019 Ataxia with Vitamin E Deficiency 55 0.068
77
SPN027 Spinal Stenosis 54 0.068
78
SPN020 Spondylosis 54 0.068
79
P PND001 Pain Disorder 49 0.068
80
LNN001 Lennox-Gastaut Syndrome 49 0.068
81
MLK003 Melkersson-Rosenthal Syndrome 48 0.068
82
P BRS044 Breast Adenocarcinoma 46 0.068
83
c TRC004 Trichorhinophalangeal Syndrome Type I 44 0.068
84
AND003 Andersen-Tawil Syndrome 43 0.068
85
KLD001 Keloids 42 0.068
86
P BNC001 Bone Carcinoma 41 0.068
87
CRY008 Cryopyrin-Associated Periodic Syndrome 36 0.068
88
HMN001 Human Monocytic Ehrlichiosis 35 0.068
89
CRB026 Cerebellar Astrocytoma 32 0.068
90
SPS057 Spasticity 29 0.068
91
DYS073 Dysphagia 28 0.068
92
FMR003 Femoral Neuropathy 26 0.068
93
c ACT066 Acute Cervicitis 22 0.068
94
c BNG076 Benign Exophthalmos Syndrome 21 0.068
95
P LFR001 Li-Fraumeni Syndrome 93 0.048
96
P RHM011 Rheumatoid Arthritis 91 0.048
97
MNK001 Menkes Disease 81 0.048
98
GLN003 Glanzmann's Thrombasthenia 80 0.048
99
P ART022 Arthritis 75 0.048
100
FBR011 Fibrodysplasia Ossificans Progressiva 75 0.048
101
ATS001 Autistic Disorder 72 0.048
102
HYP042 Hypochondroplasia 70 0.048
103
NLP001 Nail-Patella Syndrome 70 0.048
104
CRY002 Cryptorchidism 66 0.048
105
ELL001 Ellis-Van Creveld Syndrome 64 0.048
106
P CTS001 Cutis Laxa 63 0.048
107
c ACT073 Acute Leukemia 62 0.048
108
P CWD006 Cowden Syndrome 1 61 0.048
109
INT051 Intussusception 59 0.048
110
P DWR001 Dwarfism 58 0.048
111
ANR008 Aneurysm Disease 57 0.048
112
P SHR002 Short Stature 57 0.048
113
OST015 Osteochondrodysplasia 57 0.048
114
GYN001 Gynecomastia 57 0.048
115
HST009 Histiocytoma 56 0.048
116
OST014 Osteopoikilosis 56 0.048
117
WGR001 Wagr Syndrome 56 0.048
118
FBR003 Fibrous Histiocytoma 55 0.048
119
CLC006 Calcinosis 55 0.048
120
HMP005 Hemiplegia 54 0.048
121
HYP017 Hypophosphatemia 53 0.048
122
DRM004 Dermatofibrosarcoma 53 0.048
123
P SPN052 Spondyloarthropathy 52 0.048
124
HYP077 Hypertrichosis 51 0.048
125
OST003 Osteonecrosis 51 0.048
126
c SYN005 Synostosis 51 0.048
127
P DNT009 Dentin Dysplasia 49 0.048
128
DYS018 Dysostosis 49 0.048
129
P OTS001 Otosclerosis 46 0.048
130
INC001 Incontinentia Pigmenti Achromians 46 0.048
131
PSD014 Pseudopseudohypoparathyroidism 45 0.048
132
RCR001 Recurrent Corneal Erosion 44 0.048
133
PRT093 Proteus Syndrome, Somatic 44 0.048
134
c FTL001 Fetal Alcohol Syndrome 44 0.048
135
INT052 Intestinal Volvulus 42 0.048
136
c CRN035 Cranial Nerve Palsy 41 0.048
137
PRL008 Paralytic Ileus 39 0.048
138
TTH001 Tooth Ankylosis 37 0.048
139
HRD086 Hereditary Hypophosphatemic Rickets 36 0.048
140
MNT147 Mental Retardation 35 0.048
141
MTR001 Mature Cataract 34 0.048
142
ADS002 Adie Syndrome 33 0.048
143
SPN253 Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1, with or Without Fractures 30 0.048
144
BZX002 Bazex-Dupre-Christol Syndrome 29 0.048
145
c STC007 Stickler Syndrome, Type 3 29 0.048
146
c ENL009 Enlarged Parietal Foramina 27 0.048
147
OCL034 Oculocerebrocutaneous Syndrome 26 0.048
148
HYP299 Hyperostosis, Endosteal 24 0.048
149
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 20 0.048
150
UPN001 Upington Disease 19 0.048
151
AND005 Androgen Insensitivity Syndrome, Mild 18 0.048
152
BRC027 Brachydactyly Mononen Type 17 0.048
153
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 14 0.048
154
MCR070 Microcornea, Glaucoma, and Absent Frontal Sinuses 14 0.048
155
OTP003 Oto-Palatal-Digital Syndrome 13 0.048
156
c TWS001 Twist1-Related Craniosynostosis 13 0.048
157
c CTR006 Cataract Anterior Polar Dominant 13 0.048
158
DYS134 Dysspondyloenchondromatosis 11 0.048
159
c 8P2001 8p23.1 Microduplication Syndrome 11 0.048