Search results for "exostoses"

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

141 hits were found for 'exostoses'

# Family MCID Name MIFTS Score
1
c HRD001 Hereditary Multiple Exostoses 57 9.680
2
P HRD104 Hereditary Multiple Osteochondromas 33 5.771
3
P EXS004 Exostoses, Multiple, Type 1 39 4.917
4
SPS051 Spasticity Multiple Exostoses 3 4.365
5
EXS003 Exostoses Anetodermia Brachydactyly Type E 13 4.324
6
c EXS006 Exostoses, Multiple, Type 3 11 4.301
7
c EXS005 Exostoses, Multiple, Type 2 12 3.775
8
CRN096 Craniosynostosis Exostoses Nevus Epibulbar Dermoid 1 3.073
9
EXS001 Exostosis 52 2.451
10
DPY002 Dupuytren Subungual Exostosis 2 2.150
11
c OST028 Osteochondroma 54 0.235
12
P CRV039 Cervicitis 58 0.194
13
P CHN012 Chondrosarcoma 63 0.158
14
MNT147 Mental Retardation 52 0.142
15
P TRC085 Trichorhinophalangeal Syndrome Type Ii 49 0.132
16
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.123
17
PTC001 Potocki-Shaffer Syndrome 37 0.112
18
ANK002 Ankylosing Spondylitis 77 0.100
19
P SHR002 Short Stature 68 0.100
20
c BRC006 Brachydactyly 57 0.100
21
LRW002 Leri Weill Dyschondrosteosis 43 0.100
22
P LKM002 Leukemia 77 0.087
23
ACN002 Acanthosis Nigricans 63 0.087
24
NRP001 Neuropathy 62 0.087
25
PRC012 Pericardial Effusion 58 0.087
26
SPN051 Spondylitis 58 0.087
27
SCN006 Secondary Syphilis 57 0.087
28
MNN014 Mononeuritis 51 0.087
29
ANR040 Aneurysm 46 0.087
30
P ATX010 Ataxia Neuropathy Spectrum 43 0.087
31
SPS057 Spasticity 38 0.087
32
SYN053 Syndromic Diarrhea 34 0.087
33
P ACT019 Acute Myeloid Leukemia 93 0.071
34
P ATX002 Ataxia Telangiectasia 87 0.071
35
P SCH015 Schizophrenia 82 0.071
36
P OST018 Osteosarcoma 82 0.071
37
AND002 Androgen Insensitivity Syndrome 80 0.071
38
c MYL006 Myeloid Leukemia 75 0.071
39
MNK001 Menkes Disease 74 0.071
40
P ANG001 Angelman Syndrome 70 0.071
41
c CRN037 Craniosynostosis 70 0.071
42
c AXN002 Axenfeld-Rieger Syndrome 67 0.071
43
OLL001 Ollier Disease 66 0.071
44
ART019 Aortic Valve Stenosis 64 0.071
45
PSR002 Psoriasis 63 0.071
46
P ACT101 Acute Lymphoblastic Leukemia 63 0.071
47
OCC006 Occipital Horn Syndrome 62 0.071
48
P PRT008 Proteus Syndrome 61 0.071
49
c LYM026 Lymphoblastic Leukemia 57 0.071
50
ART001 Arterial Tortuosity Syndrome 55 0.071
51
c PSD015 Pseudohypoparathyroidism 55 0.071
52
AND003 Andersen-Tawil Syndrome 54 0.071
53
THR013 Thoracic Outlet Syndrome 52 0.071
54
DYS073 Dysphagia 52 0.071
55
DYS048 Dysplasia Epiphysealis Hemimelica 41 0.071
56
c TRC004 Trichorhinophalangeal Syndrome Type I 41 0.071
57
P PRB001 Pre-B-Cell Acute Lymphoblastic Leukemia 40 0.071
58
MTC018 Metachondromatosis 33 0.071
59
FMR003 Femoral Neuropathy 25 0.071
60
c BNG076 Benign Exophthalmos Syndrome 22 0.071
61
c ACT066 Acute Cervicitis 17 0.071
62
P RHM011 Rheumatoid Arthritis 94 0.050
63
P LVR011 Liver Cancer 91 0.050
64
P OST012 Osteoarthritis 76 0.050
65
P ART022 Arthritis 75 0.050
66
GLN003 Glanzmann's Thrombasthenia 74 0.050
67
P AST007 Astrocytoma 74 0.050
68
ATS001 Autistic Disorder 71 0.050
69
GLL008 Gilles De La Tourette Syndrome 71 0.050
70
c ACT074 Acute Lymphocytic Leukemia 70 0.050
71
FBR011 Fibrodysplasia Ossificans Progressiva 70 0.050
72
NLP001 Nail-Patella Syndrome 70 0.050
73
HYP042 Hypochondroplasia 69 0.050
74
P CLN016 Colon Cancer 65 0.050
75
CRY002 Cryptorchidism 63 0.050
76
SPN027 Spinal Stenosis 63 0.050
77
XLN002 X-Linked Hypophosphatemia 63 0.050
78
CLN045 Colonic Benign Neoplasm 63 0.050
79
ELL001 Ellis-Van Creveld Syndrome 61 0.050
80
WGR001 Wagr Syndrome 60 0.050
81
P SYN007 Synovitis 60 0.050
82
SPN020 Spondylosis 60 0.050
83
P ADN016 Adenocarcinoma 59 0.050
84
MYC002 Mycobacterium Avium Complex Disease 59 0.050
85
OST014 Osteopoikilosis 59 0.050
86
OST003 Osteonecrosis 59 0.050
87
P CWD006 Cowden Syndrome 1 58 0.050
88
NTR003 Natural Killer Cell Leukemia 57 0.050
89
ANK001 Ankylosis 57 0.050
90
BNC003 Bone Cancer 56 0.050
91
P DWR001 Dwarfism 55 0.050
92
INC001 Incontinentia Pigmenti Achromians 55 0.050
93
FBR003 Fibrous Histiocytoma 55 0.050
94
HST009 Histiocytoma 55 0.050
95
c SYN005 Synostosis 54 0.050
96
LNN001 Lennox-Gastaut Syndrome 54 0.050
97
P OTS001 Otosclerosis 53 0.050
98
CLC006 Calcinosis 53 0.050
99
PRC013 Pericarditis 53 0.050
100
HMP005 Hemiplegia 53 0.050
101
P PND001 Pain Disorder 52 0.050
102
MLK003 Melkersson-Rosenthal Syndrome 51 0.050
103
HYP077 Hypertrichosis 50 0.050
104
HYP017 Hypophosphatemia 49 0.050
105
PSD014 Pseudopseudohypoparathyroidism 47 0.050
106
P BRS044 Breast Adenocarcinoma 46 0.050
107
DYS018 Dysostosis 46 0.050
108
GYN001 Gynecomastia 46 0.050
109
PRT093 Proteus Syndrome, Somatic 45 0.050
110
c FTL001 Fetal Alcohol Syndrome 45 0.050
111
c BRC013 Brachydactyly Type E 45 0.050
112
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.050
113
OST015 Osteochondrodysplasia 44 0.050
114
c HRD086 Hereditary Hypophosphatemic Rickets 42 0.050
115
TTH001 Tooth Ankylosis 38 0.050
116
HMN001 Human Monocytic Ehrlichiosis 37 0.050
117
SKL017 Skeletal Dysplasias 36 0.050
118
ADS002 Adie Syndrome 35 0.050
119
KLD001 Keloids 34 0.050
120
IMM088 Immunodeficiency 36 34 0.050
121
c ENL009 Enlarged Parietal Foramina 33 0.050
122
OCL034 Oculocerebrocutaneous Syndrome 32 0.050
123
P CRN035 Cranial Nerve Palsy 32 0.050
124
c STC007 Stickler Syndrome, Type 3 31 0.050
125
KLD003 Keloid Formation 30 0.050
126
BZX002 Bazex-Dupre-Christol Syndrome 29 0.050
127
HNM002 Hinman Syndrome 28 0.050
128
SPN253 Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1, with or Without Fractures 27 0.050
129
CRB026 Cerebellar Astrocytoma 26 0.050
130
SHL001 Shoulder Impingement Syndrome 23 0.050
131
HYP299 Hyperostosis, Endosteal 22 0.050
132
AND005 Androgen Insensitivity Syndrome, Mild 21 0.050
133
UPN001 Upington Disease 20 0.050
134
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 20 0.050
135
LTH004 Lathyrism 19 0.050
136
DYS134 Dysspondyloenchondromatosis 18 0.050
137
BRC027 Brachydactyly Mononen Type 18 0.050
138
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 17 0.050
139
OTP003 Oto-Palatal-Digital Syndrome 17 0.050
140
MCR070 Microcornea, Glaucoma, and Absent Frontal Sinuses 15 0.050
141
c 8P2001 8p23.1 Microduplication Syndrome 13 0.050