Search results for "osteolysis"

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

205 hits were found for 'osteolysis'

# Family MCID Name MIFTS Score
1
OST079 Osteolysis, Familial Expansile 22 5.957
2
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 39 5.562
3
GRH001 Gorham's Disease 27 5.459
4
MLT033 Multicentric Osteolysis Nephropathy 15 5.059
5
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 16 4.302
6
PTT018 Petit-Fryns Syndrome 11 3.790
7
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 9 3.772
8
OST045 Osteolysis Syndrome Recessive 8 3.312
9
TRG005 Torg Winchester Syndrome 14 3.293
10
HJD001 Hajdu-Cheney Syndrome 42 2.858
11
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 5 2.761
12
TLP005 Talo-Patello-Scaphoid Osteolysis 10 2.744
13
CRP008 Carpo Tarsal Osteolysis Recessive 2 2.704
14
c MLT138 Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum 6 2.680
15
MLT064 Multicentric Osteolysis of Torg 4 2.680
16
VNB002 Van Bogaert-Hozay Syndrome 8 2.652
17
PHL009 Phalangeal Microgeodic Syndrome 10 1.912
18
NST002 Nestor-Guillermo Progeria Syndrome 21 1.875
19
PNT007 Penttinen-Aula Syndrome 7 1.875
20
P ART022 Arthritis 65 0.140
21
P BRS047 Breast Cancer 90 0.132
22
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.132
23
P MYL007 Myeloma 53 0.125
24
P ART023 Arthropathy 54 0.117
25
WNC001 Winchester Syndrome 34 0.117
26
MND007 Mandibuloacral Dysplasia 57 0.108
27
P TRC086 Trichohepatoenteric Syndrome 1 39 0.108
28
P OST002 Osteoporosis 71 0.099
29
c SCN006 Secondary Syphilis 51 0.099
30
SYN007 Synovitis 51 0.099
31
SCH016 Schimke Immunoosseous Dysplasia 46 0.099
32
TTR016 Tetra-Amelia Syndrome 36 0.099
33
P PRS040 Prostate Cancer 84 0.088
34
c MLT019 Multiple Myeloma 75 0.088
35
P SCL016 Scleroderma 76 0.088
36
PRG004 Progeria 61 0.088
37
LNG024 Langerhans-Cell Histiocytosis 51 0.088
38
PRS047 Prostatitis 51 0.088
39
P EXP004 Exophthalmos 47 0.088
40
MNN014 Mononeuritis 43 0.088
41
ANG037 Angiomatosis 33 0.088
42
P RHM011 Rheumatoid Arthritis 94 0.076
43
P PRD008 Periodontitis 59 0.076
44
c SYS005 Systemic Scleroderma 58 0.076
45
P HYP004 Hypercalcemia 57 0.076
46
PYC001 Pycnodysostosis 55 0.076
47
P CRV039 Cervicitis 49 0.076
48
P GCH001 Gaucher's Disease 70 0.062
49
P PRM002 Primary Hyperoxaluria 68 0.062
50
P OST001 Osteopetrosis 65 0.062
51
CYS008 Cystic Echinococcosis 64 0.062
52
PGT005 Paget Disease of Bone 65 0.062
53
RLP001 Relapsing Polychondritis 63 0.062
54
SRC014 Sarcoma 61 0.062
55
P HMN010 Hemangioma 60 0.062
56
PLY017 Polyarteritis Nodosa 60 0.062
57
c SYS004 Systemic Mastocytosis 60 0.062
58
ALV002 Alveolar Echinococcosis 60 0.062
59
ERD001 Erdheim-Chester Disease 58 0.062
60
DFF003 Diffuse Scleroderma 57 0.062
61
VSC011 Vasculitis 57 0.062
62
MXD005 Mixed Connective Tissue Disease 56 0.062
63
OCC006 Occipital Horn Syndrome 55 0.062
64
FLT001 Felty's Syndrome 55 0.062
65
c DYS166 Dysautonomia, Familial 56 0.062
66
P EPN002 Ependymoma 55 0.062
67
BSL036 Basal Cell Nevus Syndrome 55 0.062
68
OLL001 Ollier Disease 53 0.062
69
GNG013 Gingivitis 52 0.062
70
P AGM001 Agammaglobulinemia 59 0.062
71
SPH001 Sapho Syndrome 52 0.062
72
MYC002 Mycobacterium Avium Complex Disease 51 0.062
73
LYM019 Lymphosarcoma 50 0.062
74
NTR003 Natural Killer Cell Leukemia 49 0.062
75
ANK001 Ankylosis 48 0.062
76
P GNT008 Giant Cell Tumor 47 0.062
77
PPL049 Papillon-Lefevre Syndrome 48 0.062
78
c JVN016 Juvenile Hyaline Fibromatosis 47 0.062
79
c EHL057 Ehlers-Danlos Syndrome, Type Iv 48 0.062
80
KDS001 Kid Syndrome 46 0.062
81
P MNT147 Mental Retardation 46 0.062
82
P INF049 Infantile Myofibromatosis 46 0.062
83
c PND001 Pain Disorder 46 0.062
84
VHW001 Vohwinkel Syndrome 46 0.062
85
JNT002 Joint Disorders 46 0.062
86
c GCH015 Gaucher Disease, Type I 46 0.062
87
GNG012 Gingival Overgrowth 44 0.062
88
DSM003 Desmoid Disease, Hereditary 44 0.062
89
PRT039 Proteinuria 43 0.062
90
CHR288 Chronic Recurrent Multifocal Osteomyelitis 42 0.062
91
MYX001 Myxopapillary Ependymoma 42 0.062
92
c EHL055 Ehlers-Danlos Syndrome, Type Iii 43 0.062
93
MFF001 Maffucci Syndrome 42 0.062
94
P MSC022 Mosaic Variegated Aneuploidy Syndrome 40 0.062
95
c GMM003 Gamma Heavy Chain Disease 39 0.062
96
KRT012 Keratoderma 39 0.062
97
INC011 Incontinentia Pigmenti, Type Ii 40 0.062
98
P NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 39 0.062
99
OLM001 Olmsted Syndrome 37 0.062
100
HMM002 Haim-Munk Syndrome 35 0.062
101
P HYP087 Hypotrichosis 35 0.062
102
c EXS004 Exostoses, Multiple, Type 1 35 0.062
103
c GCH017 Gaucher Disease, Type Iii 34 0.062
104
LYM095 Lymphangiomatosis 32 0.062
105
KLD001 Keloids 31 0.062
106
ADS002 Adie Syndrome 30 0.062
107
MLD003 Meleda Disease 29 0.062
108
ENC010 Encephalocraniocutaneous Lipomatosis 29 0.062
109
RCK007 Rickets, Vitamin D-Resistant, Type Iia 27 0.062
110
CHM006 Chime Syndrome 28 0.062
111
TRL002 Tarlov Cysts 27 0.062
112
HNM002 Hinman Syndrome 26 0.062
113
XNT009 Xanthoma Disseminatum 24 0.062
114
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 23 0.062
115
RMN002 Ramon Syndrome 23 0.062
116
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 21 0.062
117
HSH001 Hashimoto-Pritzker Syndrome 20 0.062
118
c BNG076 Benign Exophthalmos Syndrome 19 0.062
119
HDG013 Hodgkin Lymphoma, Classical 17 0.062
120
AND005 Androgen Insensitivity Syndrome, Mild 17 0.062
121
INT238 Intellectual Disability - Cataracts - Calcified Pinnae - Myopathy 16 0.062
122
DRM020 Dermatoosteolysis Kirghizian Type 16 0.062
123
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 15 0.062
124
P PLM037 Pulmonary Hypertension 85 0.044
125
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.044
126
AND015 Androgen Insensitivity 69 0.044
127
P LPR002 Leopard Syndrome 67 0.044
128
P LKM002 Leukemia 66 0.044
129
SKN016 Skin Disease 64 0.044
130
c HYP595 Hypertension, Essential 66 0.044
131
P MST009 Mastocytosis 61 0.044
132
c JVN010 Juvenile Rheumatoid Arthritis 59 0.044
133
EWN003 Ewing Sarcoma 59 0.044
134
CRY005 Cryptococcosis 58 0.044
135
P THR014 Thrombocytopenia 56 0.044
136
P EHL001 Ehlers-Danlos Syndrome 56 0.044
137
ACN002 Acanthosis Nigricans 55 0.044
138
PGM001 Pigmented Villonodular Synovitis 53 0.044
139
P NRP001 Neuropathy 52 0.044
140
DBT010 Diabetic Neuropathy 52 0.044
141
c LCL006 Localized Scleroderma 51 0.044
142
MLT016 Multicentric Reticulohistiocytosis 51 0.044
143
CNN005 Connective Tissue Disease 50 0.044
144
DFF005 Diffuse Large B-Cell Lymphoma 50 0.044
145
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.044
146
LPD010 Lipodystrophy 49 0.044
147
LYM040 Lymphoblastic Lymphoma 49 0.044
148
P SNS014 Sinusitis 56 0.044
149
ANH002 Anhidrosis 48 0.044
150
HTC002 Hutchinson-Gilford Progeria 49 0.044
151
PGT004 Paget Disease, Juvenile 48 0.044
152
HYP077 Hypertrichosis 47 0.044
153
FBR009 Fibrous Dysplasia 47 0.044
154
PRP082 Porphyria, Congenital Erythropoietic 48 0.044
155
P BCL006 B-Cell Lymphomas 47 0.044
156
PLY012 Polyhydramnios 46 0.044
157
KRT009 Keratosis 45 0.044
158
AGG002 Aggressive Systemic Mastocytosis 45 0.044
159
VLL003 Villonodular Synovitis 45 0.044
160
THR013 Thoracic Outlet Syndrome 45 0.044
161
AND010 Androgen Insensitivity, Partial, with or Without Breast Cancer 45 0.044
162
END072 Endotheliitis 44 0.044
163
PRP002 Periapical Granuloma 44 0.044
164
CLC006 Calcinosis 44 0.044
165
ERY017 Erythema Elevatum Diutinum 43 0.044
166
P TCL004 T-Cell Leukemia 43 0.044
167
SYN005 Synostosis 43 0.044
168
EXS001 Exostosis 43 0.044
169
RHM014 Rheumatoid Vasculitis 41 0.044
170
MLR003 Melorheostosis 41 0.044
171
PTY003 Pityriasis Rubra Pilaris 41 0.044
172
LYM008 Lymphangiosarcoma 41 0.044
173
ACT055 Actinomycosis 40 0.044
174
FBR019 Fibromatosis 40 0.044
175
c ADL017 Adult T-Cell Leukemia 40 0.044
176
P PRM018 Primary Hypertrophic Osteoarthropathy 39 0.044
177
EVN001 Evans' Syndrome 39 0.044
178
MDS022 Mediastinitis 39 0.044
179
P SPN052 Spondyloarthropathy 39 0.044
180
FSC004 Fasciitis 39 0.044
181
DYS018 Dysostosis 38 0.044
182
PRS037 Periostitis 38 0.044
183
TND005 Tendinitis 38 0.044
184
ANR040 Aneurysm 35 0.044
185
SPL040 Split Hand 35 0.044
186
PHC013 Phaeochromocytoma 34 0.044
187
HMP018 Hemophilic Arthropathy 34 0.044
188
ORL015 Oral Squamous Cell Carcinoma 33 0.044
189
PLM029 Palmoplantar Keratosis 33 0.044
190
MNN002 Mononeuritis Multiplex 33 0.044
191
P KRT059 Keratosis Palmoplantaris Striata 31 0.044
192
P ATX010 Ataxia Neuropathy Spectrum 29 0.044
193
RTR008 Root Resorption 29 0.044
194
c CHR013 Chronic Apical Periodontitis 28 0.044
195
P HYL004 Hyaline Fibromatosis Syndrome 27 0.044
196
CRB079 Cerebrospinal Fluid Leak 26 0.044
197
c FRN011 Frontal Sinusitis 25 0.044
198
c HYP575 Hypotrichosis 7 24 0.044
199
GNT005 Giant Hemangioma 22 0.044
200
CLC004 Calcific Tendinitis 21 0.044
201
MNS012 Monostotic Fibrous Dysplasia 20 0.044
202
PRD003 Periodontosis 18 0.044
203
P INT105 Intellectual Disability Multi-Gene Panels 15 0.044
204
c CHR040 Chronic Frontal Sinusitis 14 0.044
205
CMP053 Camptodactyly of Fingers 11 0.044