Search results for "exostoses"

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

145 hits were found for 'exostoses'

# Family MCID Name MIFTS Score
1
c HRD001 Hereditary Multiple Exostoses 56 9.666
2
P HRD104 Hereditary Multiple Osteochondromas 32 5.768
3
P EXS004 Exostoses, Multiple, Type 1 39 4.969
4
SPS051 Spasticity Multiple Exostoses 6 4.381
5
EXS003 Exostoses Anetodermia Brachydactyly Type E 14 4.363
6
c EXS006 Exostoses, Multiple, Type 3 13 4.322
7
c EXS005 Exostoses, Multiple, Type 2 15 3.832
8
CRN096 Craniosynostosis Exostoses Nevus Epibulbar Dermoid 1 3.071
9
EXS001 Exostosis 51 2.447
10
DPY002 Dupuytren Subungual Exostosis 2 2.149
11
c OST028 Osteochondroma 54 0.233
12
P CRV039 Cervicitis 57 0.192
13
P CHN012 Chondrosarcoma 63 0.157
14
c MNT147 Mental Retardation 56 0.140
15
P TRC085 Trichorhinophalangeal Syndrome Type Ii 49 0.140
16
PTC001 Potocki-Shaffer Syndrome 39 0.140
17
LRW002 Leri Weill Dyschondrosteosis 43 0.131
18
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.122
19
ANK002 Ankylosing Spondylitis 76 0.099
20
P SHR002 Short Stature 68 0.099
21
OCC006 Occipital Horn Syndrome 63 0.099
22
c BRC006 Brachydactyly 60 0.099
23
MTC018 Metachondromatosis 33 0.099
24
P LKM002 Leukemia 76 0.086
25
OLL001 Ollier Disease 66 0.086
26
ACN002 Acanthosis Nigricans 64 0.086
27
NRP001 Neuropathy 61 0.086
28
PRC012 Pericardial Effusion 57 0.086
29
SPN051 Spondylitis 57 0.086
30
SCN006 Secondary Syphilis 56 0.086
31
MNN014 Mononeuritis 51 0.086
32
P ATX010 Ataxia Neuropathy Spectrum 47 0.086
33
ANR040 Aneurysm 45 0.086
34
DYS048 Dysplasia Epiphysealis Hemimelica 41 0.086
35
SPS057 Spasticity 37 0.086
36
SYN053 Syndromic Diarrhea 34 0.086
37
P ACT019 Acute Myeloid Leukemia 92 0.070
38
P ATX002 Ataxia Telangiectasia 87 0.070
39
P SCH015 Schizophrenia 84 0.070
40
P OST018 Osteosarcoma 81 0.070
41
AND002 Androgen Insensitivity Syndrome 80 0.070
42
c MYL006 Myeloid Leukemia 74 0.070
43
MNK001 Menkes Disease 74 0.070
44
P ANG001 Angelman Syndrome 71 0.070
45
NLP001 Nail-Patella Syndrome 70 0.070
46
c AXN002 Axenfeld-Rieger Syndrome 69 0.070
47
c CRN037 Craniosynostosis 69 0.070
48
P ACT101 Acute Lymphoblastic Leukemia 64 0.070
49
ART019 Aortic Valve Stenosis 63 0.070
50
PSR002 Psoriasis 62 0.070
51
P PRT008 Proteus Syndrome 60 0.070
52
P CWD006 Cowden Syndrome 1 59 0.070
53
c LYM026 Lymphoblastic Leukemia 56 0.070
54
ART001 Arterial Tortuosity Syndrome 55 0.070
55
c PSD015 Pseudohypoparathyroidism 54 0.070
56
AND003 Andersen-Tawil Syndrome 53 0.070
57
THR013 Thoracic Outlet Syndrome 52 0.070
58
DYS073 Dysphagia 51 0.070
59
PRT093 Proteus Syndrome, Somatic 46 0.070
60
c TRC004 Trichorhinophalangeal Syndrome Type I 42 0.070
61
P PRB001 Pre-B-Cell Acute Lymphoblastic Leukemia 39 0.070
62
OCL034 Oculocerebrocutaneous Syndrome 33 0.070
63
c STC007 Stickler Syndrome, Type 3 32 0.070
64
BZX002 Bazex-Dupre-Christol Syndrome 30 0.070
65
SPN253 Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1, with or Without Fractures 28 0.070
66
FMR003 Femoral Neuropathy 24 0.070
67
c BNG076 Benign Exophthalmos Syndrome 22 0.070
68
UPN001 Upington Disease 20 0.070
69
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 20 0.070
70
BRC027 Brachydactyly Mononen Type 18 0.070
71
DYS134 Dysspondyloenchondromatosis 18 0.070
72
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 18 0.070
73
c ACT066 Acute Cervicitis 17 0.070
74
c 8P2001 8p23.1 Microduplication Syndrome 14 0.070
75
P RHM011 Rheumatoid Arthritis 94 0.050
76
P LVR011 Liver Cancer 90 0.050
77
P OST012 Osteoarthritis 78 0.050
78
GLN003 Glanzmann's Thrombasthenia 76 0.050
79
P ART022 Arthritis 74 0.050
80
P AST007 Astrocytoma 72 0.050
81
GLL008 Gilles De La Tourette Syndrome 72 0.050
82
FBR011 Fibrodysplasia Ossificans Progressiva 70 0.050
83
ATS001 Autistic Disorder 70 0.050
84
HYP042 Hypochondroplasia 69 0.050
85
c ACT074 Acute Lymphocytic Leukemia 69 0.050
86
XLN002 X-Linked Hypophosphatemia 64 0.050
87
P CLN016 Colon Cancer 64 0.050
88
CRY002 Cryptorchidism 63 0.050
89
CLN045 Colonic Benign Neoplasm 63 0.050
90
SPN027 Spinal Stenosis 62 0.050
91
ELL001 Ellis-Van Creveld Syndrome 61 0.050
92
WGR001 Wagr Syndrome 60 0.050
93
P SYN007 Synovitis 59 0.050
94
SPN020 Spondylosis 59 0.050
95
OST014 Osteopoikilosis 59 0.050
96
P ADN016 Adenocarcinoma 58 0.050
97
MYC002 Mycobacterium Avium Complex Disease 58 0.050
98
OST003 Osteonecrosis 58 0.050
99
c CTS001 Cutis Laxa 57 0.050
100
INC001 Incontinentia Pigmenti Achromians 56 0.050
101
NTR003 Natural Killer Cell Leukemia 56 0.050
102
ANK001 Ankylosis 56 0.050
103
BNC003 Bone Cancer 56 0.050
104
P OTS001 Otosclerosis 55 0.050
105
P DWR001 Dwarfism 54 0.050
106
P PND001 Pain Disorder 54 0.050
107
FBR003 Fibrous Histiocytoma 54 0.050
108
HST009 Histiocytoma 54 0.050
109
c SYN005 Synostosis 54 0.050
110
HYP077 Hypertrichosis 53 0.050
111
LNN001 Lennox-Gastaut Syndrome 53 0.050
112
CLC006 Calcinosis 52 0.050
113
PRC013 Pericarditis 52 0.050
114
HMP005 Hemiplegia 52 0.050
115
MLK003 Melkersson-Rosenthal Syndrome 51 0.050
116
PSD014 Pseudopseudohypoparathyroidism 49 0.050
117
HYP017 Hypophosphatemia 48 0.050
118
c DNT009 Dentin Dysplasia 48 0.050
119
c BRC013 Brachydactyly Type E 46 0.050
120
P BRS044 Breast Adenocarcinoma 46 0.050
121
c FML169 Familial Osteochondritis Dissecans 45 0.050
122
DYS018 Dysostosis 45 0.050
123
GYN001 Gynecomastia 45 0.050
124
c FTL001 Fetal Alcohol Syndrome 44 0.050
125
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.050
126
OST015 Osteochondrodysplasia 44 0.050
127
c HRD086 Hereditary Hypophosphatemic Rickets 43 0.050
128
TTH001 Tooth Ankylosis 39 0.050
129
IMM088 Immunodeficiency 36 36 0.050
130
HMN001 Human Monocytic Ehrlichiosis 36 0.050
131
KLD001 Keloids 36 0.050
132
SKL017 Skeletal Dysplasias 35 0.050
133
ADS002 Adie Syndrome 35 0.050
134
c ENL009 Enlarged Parietal Foramina 33 0.050
135
P CRN035 Cranial Nerve Palsy 31 0.050
136
KLD003 Keloid Formation 29 0.050
137
HNM002 Hinman Syndrome 28 0.050
138
CRB026 Cerebellar Astrocytoma 25 0.050
139
HYP299 Hyperostosis, Endosteal 23 0.050
140
SHL001 Shoulder Impingement Syndrome 23 0.050
141
AND005 Androgen Insensitivity Syndrome, Mild 21 0.050
142
LTH004 Lathyrism 19 0.050
143
OTP003 Oto-Palatal-Digital Syndrome 17 0.050
144
MCR070 Microcornea, Glaucoma, and Absent Frontal Sinuses 15 0.050
145
c CRN215 Cornelia De Lange Syndrome 4 14 0.050