Search results for "exostoses"

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

148 hits were found for 'exostoses'

# Family MCID Name MIFTS Score
1
P HRD001 Hereditary Multiple Exostoses 48 8.929
2
c EXS004 Exostoses, Multiple, Type 1 35 5.704
3
c HRD104 Hereditary Multiple Osteochondromas 28 5.250
4
c EXS005 Exostoses, Multiple, Type 2 16 4.795
5
SPS051 Spasticity Multiple Exostoses 5 4.292
6
EXS003 Exostoses Anetodermia Brachydactyly Type E 11 3.721
7
c EXS006 Exostoses, Multiple, Type 3 9 3.681
8
CRN096 Craniosynostosis Exostoses Nevus Epibulbar Dermoid 1 3.023
9
EXS001 Exostosis 43 2.402
10
OLL001 Ollier Disease 53 2.169
11
DPY002 Dupuytren Subungual Exostosis 2 2.097
12
P OST028 Osteochondroma 47 0.234
13
P CRV039 Cervicitis 49 0.201
14
P CHN012 Chondrosarcoma 56 0.176
15
P TRC091 Trichorhinophalangeal Syndrome, Type Ii 44 0.162
16
PTC001 Potocki-Shaffer Syndrome 35 0.146
17
P MNT147 Mental Retardation 46 0.138
18
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.120
19
OCC006 Occipital Horn Syndrome 55 0.098
20
P BRC006 Brachydactyly 49 0.098
21
LRW001 Leri-Weill Dyschondrosteosis 42 0.098
22
ANR040 Aneurysm 35 0.098
23
MTC018 Metachondromatosis 30 0.098
24
P ATX030 Ataxia-Telangiectasia 76 0.085
25
P LKM002 Leukemia 66 0.085
26
ACN002 Acanthosis Nigricans 55 0.085
27
P AND016 Andersen Syndrome 54 0.085
28
P NRP001 Neuropathy 52 0.085
29
PRC012 Pericardial Effusion 49 0.085
30
ART001 Arterial Tortuosity Syndrome 48 0.085
31
SPN051 Spondylitis 48 0.085
32
MNN014 Mononeuritis 43 0.085
33
P TRC086 Trichohepatoenteric Syndrome 1 39 0.085
34
DYS048 Dysplasia Epiphysealis Hemimelica 35 0.085
35
SPS057 Spasticity 32 0.085
36
P ATX010 Ataxia Neuropathy Spectrum 29 0.085
37
MDL024 Madelung Deformity 21 0.085
38
P SCH015 Schizophrenia 79 0.069
39
AND015 Androgen Insensitivity 69 0.069
40
P ANG001 Angelman Syndrome 66 0.069
41
MNK001 Menkes Disease 65 0.069
42
P MYL006 Myeloid Leukemia 64 0.069
43
NLP001 Nail-Patella Syndrome 61 0.069
44
P CRN037 Craniosynostosis 60 0.069
45
P LYM026 Lymphoblastic Leukemia 55 0.069
46
P PSR002 Psoriasis 54 0.069
47
c SCN006 Secondary Syphilis 51 0.069
48
PRT093 Proteus Syndrome, Somatic 50 0.069
49
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.069
50
c SPN225 Spondyloarthropathy 1 48 0.069
51
P PSD015 Pseudohypoparathyroidism 47 0.069
52
c PND001 Pain Disorder 46 0.069
53
THR013 Thoracic Outlet Syndrome 45 0.069
54
DYS073 Dysphagia 45 0.069
55
MFF001 Maffucci Syndrome 42 0.069
56
c TRC092 Trichorhinophalangeal Syndrome, Type I 34 0.069
57
c ART101 Aortic Valve Disease 2 32 0.069
58
BZX001 Bazex Syndrome 31 0.069
59
OCL034 Oculocerebrocutaneous Syndrome 29 0.069
60
c STC014 Stickler Syndrome, Type Iii 29 0.069
61
c JVN024 Juvenile Hereditary Hemochromatosis 25 0.069
62
P PRT063 Proteus-Like Syndrome 25 0.069
63
P SPN127 Spondyloepimetaphyseal Dysplasia Joint Laxity 21 0.069
64
FMR003 Femoral Neuropathy 20 0.069
65
c BNG076 Benign Exophthalmos Syndrome 19 0.069
66
DYS134 Dysspondyloenchondromatosis 17 0.069
67
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 18 0.069
68
8P2002 8p23.1 Duplication Syndrome 16 0.069
69
UPN001 Upington Disease 17 0.069
70
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 16 0.069
71
OTP003 Oto-Palatal-Digital Syndrome 14 0.069
72
BRC027 Brachydactyly Mononen Type 15 0.069
73
c ACT066 Acute Cervicitis 14 0.069
74
HPT023 Hepatocellular Carcinoma 95 0.049
75
P CLR023 Colorectal Cancer 96 0.049
76
P RHM011 Rheumatoid Arthritis 94 0.049
77
P DBT085 Diabetes Mellitus, Insulin-Dependent 83 0.049
78
P OST012 Osteoarthritis 80 0.049
79
c LKM061 Leukemia, Acute Myeloid 69 0.049
80
P ART022 Arthritis 65 0.049
81
GLL008 Gilles De La Tourette Syndrome 64 0.049
82
P AST007 Astrocytoma 63 0.049
83
GLN010 Glanzmann Thrombasthenia 63 0.049
84
FBR011 Fibrodysplasia Ossificans Progressiva 61 0.049
85
HYP042 Hypochondroplasia 61 0.049
86
ATS001 Autistic Disorder 61 0.049
87
P OST009 Osteochondritis Dissecans 59 0.049
88
WGR001 Wagr Syndrome 57 0.049
89
c LKM062 Leukemia, Acute Lymphoblastic 58 0.049
90
CRY002 Cryptorchidism 57 0.049
91
OST085 Osteosarcoma, Somatic 55 0.049
92
P FTL001 Fetal Alcohol Syndrome 54 0.049
93
ELL001 Ellis-Van Creveld Syndrome 53 0.049
94
SPN027 Spinal Stenosis 53 0.049
95
MYC002 Mycobacterium Avium Complex Disease 51 0.049
96
SPN020 Spondylosis 51 0.049
97
SYN007 Synovitis 51 0.049
98
BNC003 Bone Cancer 50 0.049
99
P CTS001 Cutis Laxa 50 0.049
100
OST003 Osteonecrosis 49 0.049
101
P ADN016 Adenocarcinoma 49 0.049
102
NTR003 Natural Killer Cell Leukemia 49 0.049
103
P HYP613 Hypophosphatemic Rickets 49 0.049
104
ANK001 Ankylosis 48 0.049
105
DWR001 Dwarfism 48 0.049
106
HYP077 Hypertrichosis 47 0.049
107
P OTS001 Otosclerosis 46 0.049
108
HST009 Histiocytoma 46 0.049
109
FBR003 Fibrous Histiocytoma 46 0.049
110
LNN001 Lennox-Gastaut Syndrome 46 0.049
111
PRC013 Pericarditis 45 0.049
112
HMP005 Hemiplegia 44 0.049
113
P SCL018 Scoliosis 45 0.049
114
CLC006 Calcinosis 44 0.049
115
MLK003 Melkersson-Rosenthal Syndrome 44 0.049
116
PSD014 Pseudopseudohypoparathyroidism 43 0.049
117
SYN005 Synostosis 43 0.049
118
P DNT009 Dentin Dysplasia 42 0.049
119
HYP017 Hypophosphatemia 42 0.049
120
c BRC082 Brachydactyly, Type E 42 0.049
121
P CHN059 Chondrocalcinosis 41 0.049
122
P BRS044 Breast Adenocarcinoma 39 0.049
123
c HRD086 Hereditary Hypophosphatemic Rickets 39 0.049
124
DYS018 Dysostosis 38 0.049
125
OST015 Osteochondrodysplasia 38 0.049
126
GYN001 Gynecomastia 37 0.049
127
INC001 Incontinentia Pigmenti Achromians 36 0.049
128
TTH001 Tooth Ankylosis 33 0.049
129
KLD001 Keloids 31 0.049
130
SKL017 Skeletal Dysplasias 30 0.049
131
HYP299 Hyperostosis, Endosteal 30 0.049
132
PSL001 Pasli Disease 30 0.049
133
ADS002 Adie Syndrome 30 0.049
134
HMN001 Human Monocytic Ehrlichiosis 29 0.049
135
c ACT115 Acute Myeloid Leukemia, Adult 27 0.049
136
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.049
137
TFT003 Tufting Enteropathy 26 0.049
138
P CRN035 Cranial Nerve Palsy 26 0.049
139
KLD003 Keloid Formation 25 0.049
140
HNM002 Hinman Syndrome 26 0.049
141
CRB026 Cerebellar Astrocytoma 20 0.049
142
SHL001 Shoulder Impingement Syndrome 18 0.049
143
AND005 Androgen Insensitivity Syndrome, Mild 17 0.049
144
LTH004 Lathyrism 17 0.049
145
c CRN215 Cornelia De Lange Syndrome 4 15 0.049
146
MCR070 Microcornea, Glaucoma, and Absent Frontal Sinuses 13 0.049
147
OST076 Osteochondritis Dissecans, Short Stature, and Early-Onset Osteoarthritis 12 0.049
148
DVL012 Developmental Dysplasia of the Hip 1 12 0.049