Search results for "exostoses"

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

136 hits were found for 'exostoses'

# Family MCID Name MIFTS Score
1
c HRD001 Hereditary Multiple Exostoses 55 8.522
2
P EXS004 Exostoses, Multiple, Type 1 38 4.416
3
P HRD104 Hereditary Multiple Osteochondromas 32 4.400
4
EXS003 Exostoses Anetodermia Brachydactyly Type E 13 4.322
5
c EXS006 Exostoses, Multiple, Type 3 11 4.299
6
SPS051 Spasticity Multiple Exostoses 3 3.795
7
c EXS005 Exostoses, Multiple, Type 2 12 3.774
8
CRN096 Craniosynostosis Exostoses Nevus Epibulbar Dermoid 1 3.072
9
EXS001 Exostosis 51 2.465
10
DPY002 Dupuytren Subungual Exostosis 2 2.149
11
c OST028 Osteochondroma 54 0.237
12
P CRV039 Cervicitis 57 0.196
13
P CHN012 Chondrosarcoma 63 0.160
14
MNT147 Mental Retardation 51 0.143
15
P SHR002 Short Stature 64 0.101
16
c BRC006 Brachydactyly 55 0.101
17
P TRC085 Trichorhinophalangeal Syndrome Type Ii 46 0.101
18
LRW002 Leri Weill Dyschondrosteosis 42 0.101
19
PTC001 Potocki-Shaffer Syndrome 36 0.101
20
ANK002 Ankylosing Spondylitis 74 0.088
21
ACN002 Acanthosis Nigricans 69 0.088
22
NRP001 Neuropathy 61 0.088
23
PRC012 Pericardial Effusion 58 0.088
24
SCN006 Secondary Syphilis 57 0.088
25
MNN014 Mononeuritis 51 0.088
26
ANR040 Aneurysm 44 0.088
27
P ATX010 Ataxia Neuropathy Spectrum 41 0.088
28
SPS057 Spasticity 37 0.088
29
SYN053 Syndromic Diarrhea 32 0.088
30
P ACT019 Acute Myeloid Leukemia 92 0.072
31
P SCH015 Schizophrenia 82 0.072
32
AND002 Androgen Insensitivity Syndrome 80 0.072
33
P OST018 Osteosarcoma 79 0.072
34
P LKM002 Leukemia 77 0.072
35
c MYL006 Myeloid Leukemia 72 0.072
36
P ANG001 Angelman Syndrome 70 0.072
37
c CRN037 Craniosynostosis 70 0.072
38
c AXN002 Axenfeld-Rieger Syndrome 66 0.072
39
OLL001 Ollier Disease 66 0.072
40
ART019 Aortic Valve Stenosis 64 0.072
41
PSR002 Psoriasis 63 0.072
42
OCC006 Occipital Horn Syndrome 62 0.072
43
P PRT008 Proteus Syndrome 57 0.072
44
SPN051 Spondylitis 57 0.072
45
c PSD015 Pseudohypoparathyroidism 54 0.072
46
THR013 Thoracic Outlet Syndrome 52 0.072
47
DYS073 Dysphagia 51 0.072
48
DYS048 Dysplasia Epiphysealis Hemimelica 41 0.072
49
c TRC004 Trichorhinophalangeal Syndrome Type I 40 0.072
50
MTC018 Metachondromatosis 33 0.072
51
FMR003 Femoral Neuropathy 26 0.072
52
c BNG076 Benign Exophthalmos Syndrome 22 0.072
53
c ACT066 Acute Cervicitis 18 0.072
54
P RHM011 Rheumatoid Arthritis 93 0.051
55
P ATX002 Ataxia Telangiectasia 86 0.051
56
HPT023 Hepatocellular Carcinoma 79 0.051
57
P CLN016 Colon Cancer 78 0.051
58
P OST012 Osteoarthritis 75 0.051
59
P ART022 Arthritis 75 0.051
60
GLN003 Glanzmann's Thrombasthenia 73 0.051
61
MNK001 Menkes Disease 73 0.051
62
P AST007 Astrocytoma 71 0.051
63
ATS001 Autistic Disorder 71 0.051
64
GLL008 Gilles De La Tourette Syndrome 70 0.051
65
HYP042 Hypochondroplasia 69 0.051
66
FBR011 Fibrodysplasia Ossificans Progressiva 69 0.051
67
NLP001 Nail-Patella Syndrome 69 0.051
68
CRY002 Cryptorchidism 63 0.051
69
SPN027 Spinal Stenosis 62 0.051
70
ELL001 Ellis-Van Creveld Syndrome 60 0.051
71
WGR001 Wagr Syndrome 59 0.051
72
P SYN007 Synovitis 59 0.051
73
SPN020 Spondylosis 59 0.051
74
OST014 Osteopoikilosis 58 0.051
75
MYC002 Mycobacterium Avium Complex Disease 58 0.051
76
OST003 Osteonecrosis 58 0.051
77
P CWD006 Cowden Syndrome 1 58 0.051
78
P ADN016 Adenocarcinoma 58 0.051
79
NTR003 Natural Killer Cell Leukemia 57 0.051
80
ANK001 Ankylosis 57 0.051
81
c CTS001 Cutis Laxa 55 0.051
82
HST009 Histiocytoma 55 0.051
83
P DWR001 Dwarfism 55 0.051
84
FBR003 Fibrous Histiocytoma 54 0.051
85
c SYN005 Synostosis 54 0.051
86
ART001 Arterial Tortuosity Syndrome 54 0.051
87
LNN001 Lennox-Gastaut Syndrome 53 0.051
88
PRC013 Pericarditis 53 0.051
89
P OTS001 Otosclerosis 53 0.051
90
AND003 Andersen-Tawil Syndrome 53 0.051
91
HMP005 Hemiplegia 52 0.051
92
DRM004 Dermatofibrosarcoma 52 0.051
93
c DNT009 Dentin Dysplasia 51 0.051
94
CLC006 Calcinosis 51 0.051
95
MLK003 Melkersson-Rosenthal Syndrome 50 0.051
96
HYP077 Hypertrichosis 49 0.051
97
P PND001 Pain Disorder 48 0.051
98
HYP017 Hypophosphatemia 48 0.051
99
PSD014 Pseudopseudohypoparathyroidism 46 0.051
100
GYN001 Gynecomastia 46 0.051
101
PRT093 Proteus Syndrome, Somatic 45 0.051
102
DYS018 Dysostosis 45 0.051
103
c BRC013 Brachydactyly Type E 45 0.051
104
OST015 Osteochondrodysplasia 45 0.051
105
c FTL001 Fetal Alcohol Syndrome 45 0.051
106
INC001 Incontinentia Pigmenti Achromians 43 0.051
107
P BRS044 Breast Adenocarcinoma 42 0.051
108
c HRD086 Hereditary Hypophosphatemic Rickets 41 0.051
109
SKL017 Skeletal Dysplasias 39 0.051
110
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.051
111
TTH001 Tooth Ankylosis 38 0.051
112
HMN001 Human Monocytic Ehrlichiosis 36 0.051
113
ADS002 Adie Syndrome 35 0.051
114
KLD001 Keloids 34 0.051
115
OCL034 Oculocerebrocutaneous Syndrome 32 0.051
116
c ENL009 Enlarged Parietal Foramina 32 0.051
117
c CRN035 Cranial Nerve Palsy 31 0.051
118
c STC007 Stickler Syndrome, Type 3 30 0.051
119
BZX002 Bazex-Dupre-Christol Syndrome 30 0.051
120
KLD003 Keloid Formation 28 0.051
121
HNM002 Hinman Syndrome 27 0.051
122
PSL001 Pasli Disease 27 0.051
123
SPN253 Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1, with or Without Fractures 27 0.051
124
CRB026 Cerebellar Astrocytoma 25 0.051
125
SHL001 Shoulder Impingement Syndrome 24 0.051
126
HYP299 Hyperostosis, Endosteal 22 0.051
127
AND005 Androgen Insensitivity Syndrome, Mild 21 0.051
128
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 20 0.051
129
UPN001 Upington Disease 19 0.051
130
LTH004 Lathyrism 19 0.051
131
BRC027 Brachydactyly Mononen Type 17 0.051
132
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 17 0.051
133
DYS134 Dysspondyloenchondromatosis 17 0.051
134
OTP003 Oto-Palatal-Digital Syndrome 16 0.051
135
MCR070 Microcornea, Glaucoma, and Absent Frontal Sinuses 15 0.051
136
c 8P2001 8p23.1 Microduplication Syndrome 13 0.051