Search results for osteolysis

258 hits were found for osteolysis

# Family MCID Name MIFTS Score
1
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 41 7.905
2
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 50 7.680
3
FML345 Familial Expansile Osteolysis 45 6.658
4
OST149 Osteolysis Syndrome, Recessive 19 4.673
5
GRH001 Gorham's Disease 37 4.314
6
NST002 Nestor-Guillermo Progeria Syndrome 27 3.840
7
MLT033 Multicentric Osteolysis Nephropathy 9 3.828
8
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 11 3.757
9
HJD001 Hajdu-Cheney Syndrome 64 3.455
10
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 15 3.427
11
CYS041 Cystic Angiomatosis of Bone, Diffuse 26 3.243
12
OSB002 Osebold Skeletal Dysplasia/osteolysis Syndrome 6 2.678
13
P ACR062 Acroosteolysis 35 1.961
14
PTT018 Petit-Fryns Syndrome 12 1.961
15
IDP078 Idiopathic Phalangeal Acro-Osteolysis 7 1.942
16
CRP008 Carpo Tarsal Osteolysis Recessive 2 1.942
17
c MLT138 Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum 7 1.920
18
PHL009 Phalangeal Microgeodic Syndrome 12 1.894
19
PNT007 Penttinen-Aula Syndrome 9 1.894
20
VNB002 Van Bogaert-Hozay Syndrome 13 1.860
21
c ACR044 Acroosteolysis Dominant Type 29 0.169
22
P BRS047 Breast Cancer 100 0.154
23
P ART023 Arthropathy 68 0.142
24
WNC001 Winchester Syndrome 37 0.136
25
P ART022 Arthritis 77 0.123
26
P OST002 Osteoporosis 75 0.116
27
P PRS040 Prostate Cancer 88 0.109
28
P GNT008 Giant Cell Tumor 49 0.109
29
CHN070 Cohen-Gibson Syndrome 51 0.101
30
MYL069 Myeloma, Multiple 86 0.092
31
PRS047 Prostatitis 59 0.092
32
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.092
33
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.092
34
OST159 Osteogenic Sarcoma 70 0.082
35
SRC014 Sarcoma 68 0.082
36
c SCL052 Scleroderma, Familial Progressive 60 0.082
37
CLC006 Calcinosis 51 0.082
38
PYC001 Pycnodysostosis 51 0.082
39
P CRV039 Cervicitis 49 0.082
40
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 42 0.082
41
HYL004 Hyaline Fibromatosis Syndrome 40 0.082
42
ANG037 Angiomatosis 36 0.082
43
DRM042 Dermatoosteolysis, Kirghizian Type 20 0.082
44
P LYM118 Lymphoma 71 0.071
45
P OST001 Osteopetrosis 70 0.071
46
P ANR048 Aniridia 1 68 0.071
47
SYN007 Synovitis 61 0.071
48
P HYP726 Hypercalcemia, Infantile, 1 57 0.071
49
RTR008 Root Resorption 44 0.071
50
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.071
51
FRN039 Frank-Ter Haar Syndrome 37 0.071
52
LYM095 Lymphangiomatosis 35 0.071
53
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.071
54
PGT009 Paget Disease of Bone 2, Early-Onset 24 0.071
55
c SNG011 Singleton-Merten Syndrome 1 23 0.071
56
ANR038 Anorexia Nervosa 1 21 0.071
57
BLD137 Blood Group--Ahonen 17 0.071
58
P LNG032 Lung Cancer 99 0.058
59
OST012 Osteoarthritis 88 0.058
60
LYM133 Lymphoma, Hodgkin, Classic 78 0.058
61
c SPN225 Spondyloarthropathy 1 71 0.058
62
P AGM001 Agammaglobulinemia 70 0.058
63
P SYS005 Systemic Scleroderma 67 0.058
64
P PRD008 Periodontitis 67 0.058
65
MXD005 Mixed Connective Tissue Disease 66 0.058
66
VSC011 Vasculitis 66 0.058
67
SYS004 Systemic Mastocytosis 65 0.058
68
DSM004 Desmoid Tumor 63 0.058
69
OST003 Osteonecrosis 63 0.058
70
HTC003 Hutchinson-Gilford Progeria Syndrome 62 0.058
71
P GCH001 Gaucher's Disease 62 0.058
72
P HMN010 Hemangioma 61 0.058
73
PGT001 Paget's Disease of Bone 60 0.058
74
JNT002 Joint Disorders 60 0.058
75
P HST010 Histiocytosis 60 0.058
76
BNC003 Bone Cancer 59 0.058
77
LYM019 Lymphosarcoma 58 0.058
78
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 57 0.058
79
INC021 Incontinentia Pigmenti 57 0.058
80
c GCH015 Gaucher Disease, Type I 57 0.058
81
ERD001 Erdheim-Chester Disease 57 0.058
82
P EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.058
83
PRP082 Porphyria, Congenital Erythropoietic 56 0.058
84
CHR288 Chronic Recurrent Multifocal Osteomyelitis 55 0.058
85
END081 Endosteal Hyperostosis, Autosomal Dominant 55 0.058
86
ENC044 Enchondromatosis, Multiple, Ollier Type 54 0.058
87
SPH001 Sapho Syndrome 54 0.058
88
P EPN002 Ependymoma 53 0.058
89
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.058
90
DFF035 Diffuse Cutaneous Systemic Sclerosis 53 0.058
91
HPT082 Hepatic Adenomas, Familial 52 0.058
92
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 51 0.058
93
MLT145 Multiple Enchondromatosis, Maffucci Type 51 0.058
94
FLT011 Felty Syndrome 51 0.058
95
KLD001 Keloids 50 0.058
96
PPL049 Papillon-Lefevre Syndrome 50 0.058
97
P INF049 Infantile Myofibromatosis 49 0.058
98
OCC006 Occipital Horn Syndrome 49 0.058
99
c PRD040 Periodontitis, Chronic 49 0.058
100
c GMM003 Gamma Heavy Chain Disease 49 0.058
101
SKL017 Skeletal Dysplasias 48 0.058
102
RSD004 Rosai-Dorfman Disease 48 0.058
103
P HYP087 Hypotrichosis 48 0.058
104
ENC010 Encephalocraniocutaneous Lipomatosis 48 0.058
105
c GCH017 Gaucher Disease, Type Iii 47 0.058
106
P MSC022 Mosaic Variegated Aneuploidy Syndrome 47 0.058
107
MLT016 Multicentric Reticulohistiocytosis 47 0.058
108
ANR009 Aneurysmal Bone Cysts 46 0.058
109
c EXS019 Exostoses, Multiple, Type I 46 0.058
110
VTM027 Vitamin D-Dependent Rickets, Type 2a 46 0.058
111
KDS001 Kid Syndrome 44 0.058
112
PGT008 Paget Disease of Bone 5, Juvenile-Onset 44 0.058
113
MYX001 Myxopapillary Ependymoma 44 0.058
114
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.058
115
PRP017 Periapical Periodontitis 42 0.058
116
P VHW001 Vohwinkel Syndrome 41 0.058
117
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.058
118
TTH008 Tooth Resorption 38 0.058
119
XNT009 Xanthoma Disseminatum 38 0.058
120
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.058
121
ESN017 Eosinophilic Granuloma 37 0.058
122
HMP018 Hemophilic Arthropathy 37 0.058
123
ACR005 Acrodermatitis 35 0.058
124
TRL002 Tarlov Cysts 34 0.058
125
PRS037 Periostitis 33 0.058
126
PRM056 Primrose Syndrome 33 0.058
127
STR096 Striate Palmoplantar Keratoderma 33 0.058
128
BNR002 Bone Resorption Disease 33 0.058
129
BNR001 Bone Remodeling Disease 31 0.058
130
c CHR013 Chronic Apical Periodontitis 31 0.058
131
ALR002 Al-Raqad Syndrome 30 0.058
132
PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 30 0.058
133
ISC005 Ischemic Bone Disease 30 0.058
134
KMM001 Kummell's Disease 28 0.058
135
RMN002 Ramon Syndrome 27 0.058
136
PRM206 Premature Aging Syndrome, Penttinen Type 25 0.058
137
BRS043 Breast Leiomyosarcoma 25 0.058
138
HSH001 Hashimoto-Pritzker Syndrome 24 0.058
139
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.058
140
P RHM011 Rheumatoid Arthritis 91 0.041
141
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.041
142
P PLM037 Pulmonary Hypertension 79 0.041
143
P LKM002 Leukemia 75 0.041
144
SQM006 Squamous Cell Carcinoma 74 0.041
145
EWN003 Ewing Sarcoma 72 0.041
146
c JVN010 Juvenile Rheumatoid Arthritis 71 0.041
147
P BCL006 B-Cell Lymphomas 70 0.041
148
LYM007 Lymphangioleiomyomatosis 68 0.041
149
c SML038 Small Cell Cancer of the Lung 67 0.041
150
c LCL006 Localized Scleroderma 66 0.041
151
P PSR002 Psoriasis 65 0.041
152
CNN005 Connective Tissue Disease 65 0.041
153
P THR014 Thrombocytopenia 65 0.041
154
AGN016 Aging 65 0.041
155
c ART101 Aortic Valve Disease 2 65 0.041
156
DFF005 Diffuse Large B-Cell Lymphoma 64 0.041
157
GNG013 Gingivitis 64 0.041
158
P NRP001 Neuropathy 63 0.041
159
RCK004 Rickets 63 0.041
160
c ADL017 Adult T-Cell Leukemia 63 0.041
161
P SNS014 Sinusitis 62 0.041
162
RHM027 Rheumatic Disease 62 0.041
163
P EHL001 Ehlers-Danlos Syndrome 61 0.041
164
P FBR017 Fibrosarcoma 61 0.041
165
P SPN052 Spondyloarthropathy 61 0.041
166
ANR040 Aneurysm 61 0.041
167
DBT010 Diabetic Neuropathy 60 0.041
168
ORL015 Oral Squamous Cell Carcinoma 59 0.041
169
P HYP069 Hyperparathyroidism 58 0.041
170
LYM040 Lymphoblastic Lymphoma 58 0.041
171
P LPR002 Leopard Syndrome 56 0.041
172
BNF002 Bone Fracture 56 0.041
173
P ACT008 Actinic Keratosis 56 0.041
174
ANK001 Ankylosis 56 0.041
175
SRS001 Serous Cystadenocarcinoma 55 0.041
176
P HYP024 Hypoparathyroidism 55 0.041
177
ADM013 Adamantinoma of Long Bones 55 0.041
178
P SHR029 Short Syndrome 54 0.041
179
ERY017 Erythema Elevatum Diutinum 54 0.041
180
CRY005 Cryptococcosis 54 0.041
181
P CLL015 Collagen Disease 53 0.041
182
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 53 0.041
183
KRT009 Keratosis 53 0.041
184
P CHL069 Cholesteatoma 52 0.041
185
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.041
186
OST011 Osteomalacia 52 0.041
187
GNG012 Gingival Overgrowth 52 0.041
188
P FNC043 Fanconi Anemia, Complementation Group E 52 0.041
189
LYM008 Lymphangiosarcoma 51 0.041
190
P PRX021 Proximal Symphalangism 51 0.041
191
PRT029 Parathyroid Adenoma 50 0.041
192
P PSD015 Pseudohypoparathyroidism 50 0.041
193
PRT030 Parathyroid Gland Disease 50 0.041
194
P TCL004 T-Cell Leukemia 50 0.041
195
RNL011 Renal Osteodystrophy 49 0.041
196
FBR009 Fibrous Dysplasia 49 0.041
197
HYP077 Hypertrichosis 49 0.041
198
AND020 Androgen Insensitivity, Partial 49 0.041
199
P PTY003 Pityriasis Rubra Pilaris 48 0.041
200
FSC004 Fasciitis 48 0.041
201
DYS018 Dysostosis 48 0.041
202
c BRN108 Branchiootic Syndrome 1 47 0.041
203
FBR019 Fibromatosis 47 0.041
204
KLT001 Klatskin's Tumor 47 0.041
205
P HRD021 Hereditary Sensory Neuropathy 47 0.041
206
PST011 Pustulosis of Palm and Sole 47 0.041
207
AGG002 Aggressive Systemic Mastocytosis 47 0.041
208
LGH004 Light Chain Deposition Disease 47 0.041
209
P PRM018 Primary Hypertrophic Osteoarthropathy 46 0.041
210
KPS002 Kaposiform Hemangioendothelioma 46 0.041
211
EXS001 Exostosis 46 0.041
212
END072 Endotheliitis 46 0.041
213
NTR003 Natural Killer Cell Leukemia 45 0.041
214
PRD003 Periodontosis 45 0.041
215
ANH002 Anhidrosis 45 0.041
216
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 45 0.041
217
MDS022 Mediastinitis 44 0.041
218
PHC013 Phaeochromocytoma 44 0.041
219
BNG036 Bone Giant Cell Tumor 44 0.041
220
c PSR021 Psoriasis 14, Pustular 44 0.041
221
HMN016 Hemangioendothelioma 43 0.041
222
ACT055 Actinomycosis 43 0.041
223
FRY002 Fryns Syndrome 43 0.041
224
MLR003 Melorheostosis 43 0.041
225
c OST131 Osteopetrosis, Autosomal Dominant 2 43 0.041
226
NDL001 Nodular Malignant Melanoma 42 0.041
227
TND005 Tendinitis 42 0.041
228
ADP007 Adie Pupil 41 0.041
229
P PST059 Pustular Psoriasis 40 0.041
230
RHM014 Rheumatoid Vasculitis 40 0.041
231
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.041
232
DSM003 Desmoid Disease, Hereditary 40 0.041
233
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 39 0.041
234
CRB079 Cerebrospinal Fluid Leak 39 0.041
235
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 38 0.041
236
ENT004 Enthesopathy 38 0.041
237
CLC004 Calcific Tendinitis 38 0.041
238
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 37 0.041
239
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.041
240
LTR009 Lateral Meningocele Syndrome 34 0.041
241
OST167 Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis 34 0.041
242
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 33 0.041
243
GNT005 Giant Hemangioma 33 0.041
244
ADR023 Adrenomyodystrophy 33 0.041
245
JWC001 Jaw Cancer 32 0.041
246
TTH001 Tooth Ankylosis 32 0.041
247
STY001 Satoyoshi Syndrome 32 0.041
248
c FRN011 Frontal Sinusitis 30 0.041
249
PGT007 Paget Disease of Bone 3 28 0.041
250
MNN002 Mononeuritis Multiplex 27 0.041
251
c MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 26 0.041
252
EXT012 Extraskeletal Chondroma 25 0.041
253
MNS012 Monostotic Fibrous Dysplasia 22 0.041
254
c CHR040 Chronic Frontal Sinusitis 20 0.041
255
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 17 0.041
256
c SNG012 Singleton-Merten Syndrome 2 17 0.041
257
PGT006 Paget Disease of Bone 4 13 0.041
258
PRG025 Progeroid Syndrome, Penttinen Type 6 0.041
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