Search results for osteolysis

226 hits were found for osteolysis

# Family MCID Name MIFTS Score
1
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 41 8.006
2
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 48 7.759
3
OST079 Osteolysis, Familial Expansile 39 6.315
4
GRH001 Gorham's Disease 35 4.362
5
OST149 Osteolysis Syndrome, Recessive 14 4.290
6
MLT033 Multicentric Osteolysis Nephropathy 11 3.879
7
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 10 3.805
8
HJD001 Hajdu-Cheney Syndrome 59 3.497
9
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 12 3.446
10
NST002 Nestor-Guillermo Progeria Syndrome 22 3.305
11
CYS041 Cystic Angiomatosis of Bone, Diffuse 27 2.690
12
MLT064 Multicentric Osteolysis of Torg 6 1.969
13
IDP078 Idiopathic Phalangeal Acro-Osteolysis 5 1.969
14
CRP008 Carpo Tarsal Osteolysis Recessive 2 1.969
15
PTT018 Petit-Fryns Syndrome 7 1.946
16
c MLT138 Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum 7 1.946
17
PHL009 Phalangeal Microgeodic Syndrome 9 1.919
18
VNB002 Van Bogaert-Hozay Syndrome 7 1.883
19
PNT007 Penttinen-Aula Syndrome 6 1.883
20
P BRS047 Breast Cancer 100 0.155
21
P ART023 Arthropathy 64 0.143
22
WNC001 Winchester Syndrome 39 0.143
23
P ART022 Arthritis 75 0.122
24
P PRS040 Prostate Cancer 90 0.114
25
P OST002 Osteoporosis 64 0.105
26
P MLT019 Multiple Myeloma 83 0.096
27
PRS047 Prostatitis 56 0.096
28
P GNT008 Giant Cell Tumor 49 0.096
29
CLC006 Calcinosis 50 0.086
30
ANG037 Angiomatosis 37 0.086
31
P LYM118 Lymphoma 69 0.075
32
P SYS005 Systemic Scleroderma 61 0.075
33
SYN007 Synovitis 58 0.075
34
MND007 Mandibuloacral Dysplasia 49 0.075
35
PYC001 Pycnodysostosis 48 0.075
36
P CRV039 Cervicitis 45 0.075
37
P MSC022 Mosaic Variegated Aneuploidy Syndrome 44 0.075
38
HYL004 Hyaline Fibromatosis Syndrome 38 0.075
39
LYM095 Lymphangiomatosis 32 0.075
40
DRM042 Dermatoosteolysis, Kirghizian Type 15 0.075
41
P LNG032 Lung Cancer 95 0.061
42
SRC014 Sarcoma 66 0.061
43
P AGM001 Agammaglobulinemia 64 0.061
44
P PRD008 Periodontitis 63 0.061
45
OST085 Osteosarcoma, Somatic 63 0.061
46
MXD005 Mixed Connective Tissue Disease 62 0.061
47
VSC011 Vasculitis 62 0.061
48
P GCH001 Gaucher's Disease 62 0.061
49
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.061
50
c SYS004 Systemic Mastocytosis 60 0.061
51
P HMN010 Hemangioma 59 0.061
52
INC021 Incontinentia Pigmenti 59 0.061
53
c GCH015 Gaucher Disease, Type I 59 0.061
54
P HST010 Histiocytosis 58 0.061
55
BNC003 Bone Cancer 58 0.061
56
HTC002 Hutchinson-Gilford Progeria 57 0.061
57
DSM004 Desmoid Tumor 56 0.061
58
JNT002 Joint Disorders 55 0.061
59
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.061
60
KDS001 Kid Syndrome 53 0.061
61
P EPN002 Ependymoma 53 0.061
62
LYM019 Lymphosarcoma 53 0.061
63
ERD001 Erdheim-Chester Disease 52 0.061
64
KLD001 Keloids 51 0.061
65
c EHL055 Ehlers-Danlos Syndrome, Type Iii 50 0.061
66
HPT074 Hepatic Adenoma, Somatic 50 0.061
67
c DYS166 Dysautonomia, Familial 49 0.061
68
P INT063 Intellectual Disability 49 0.061
69
PPL049 Papillon-Lefevre Syndrome 48 0.061
70
c GMM003 Gamma Heavy Chain Disease 46 0.061
71
P HYP087 Hypotrichosis 46 0.061
72
SPH001 Sapho Syndrome 46 0.061
73
c GCH017 Gaucher Disease, Type Iii 46 0.061
74
FLT011 Felty Syndrome 46 0.061
75
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.061
76
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.061
77
ENC044 Enchondromatosis, Multiple, Ollier Type 44 0.061
78
PRG004 Progeria 44 0.061
79
P INF049 Infantile Myofibromatosis 43 0.061
80
c HRD104 Hereditary Multiple Osteochondromas 43 0.061
81
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.061
82
VHW001 Vohwinkel Syndrome 41 0.061
83
RSD004 Rosai-Dorfman Disease 41 0.061
84
MLT145 Multiple Enchondromatosis, Maffucci Type 40 0.061
85
MYX001 Myxopapillary Ependymoma 39 0.061
86
MYH012 Myhre Syndrome 38 0.061
87
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.061
88
RCK007 Rickets, Vitamin D-Resistant, Type Iia 37 0.061
89
TTR016 Tetra-Amelia Syndrome 36 0.061
90
ALR002 Al-Raqad Syndrome 36 0.061
91
ACR005 Acrodermatitis 36 0.061
92
XNT009 Xanthoma Disseminatum 34 0.061
93
PRM056 Primrose Syndrome 32 0.061
94
RMN002 Ramon Syndrome 30 0.061
95
TRL002 Tarlov Cysts 29 0.061
96
HNM002 Hinman Syndrome 25 0.061
97
BNR002 Bone Resorption Disease 21 0.061
98
PRM206 Premature Aging Syndrome, Penttinen Type 21 0.061
99
c SNG011 Singleton-Merten Syndrome 1 18 0.061
100
AND005 Androgen Insensitivity Syndrome, Mild 16 0.061
101
ACR044 Acroosteolysis Dominant Type 16 0.061
102
HSH001 Hashimoto-Pritzker Syndrome 15 0.061
103
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 13 0.061
104
P RHM011 Rheumatoid Arthritis 89 0.043
105
P OST012 Osteoarthritis 83 0.043
106
P PLM037 Pulmonary Hypertension 79 0.043
107
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.043
108
P LKM002 Leukemia 71 0.043
109
SQM006 Squamous Cell Carcinoma 70 0.043
110
EWN003 Ewing Sarcoma 66 0.043
111
P ATR011 Atrial Fibrillation 66 0.043
112
P BCL006 B-Cell Lymphomas 65 0.043
113
P LNG028 Long Qt Syndrome 64 0.043
114
P THR014 Thrombocytopenia 64 0.043
115
P OST001 Osteopetrosis 63 0.043
116
P EHL001 Ehlers-Danlos Syndrome 63 0.043
117
CNN005 Connective Tissue Disease 62 0.043
118
c LNG044 Long Qt Syndrome 1 62 0.043
119
GNG013 Gingivitis 61 0.043
120
P PSR002 Psoriasis 61 0.043
121
P SDD001 Sudden Infant Death Syndrome 61 0.043
122
CRD119 Cardiac Arrest 61 0.043
123
P RCK004 Rickets 61 0.043
124
c LCL006 Localized Scleroderma 61 0.043
125
P SNS014 Sinusitis 60 0.043
126
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.043
127
c ADL017 Adult T-Cell Leukemia 60 0.043
128
P SPN052 Spondyloarthropathy 60 0.043
129
P BRG001 Brugada Syndrome 59 0.043
130
P NRP001 Neuropathy 59 0.043
131
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 59 0.043
132
DFF005 Diffuse Large B-Cell Lymphoma 59 0.043
133
c FML001 Familial Atrial Fibrillation 58 0.043
134
P SHR029 Short Syndrome 58 0.043
135
RHM027 Rheumatic Disease 58 0.043
136
c LNG047 Long Qt Syndrome 2 57 0.043
137
ORL015 Oral Squamous Cell Carcinoma 57 0.043
138
ANR040 Aneurysm 57 0.043
139
P HYP613 Hypophosphatemic Rickets 57 0.043
140
P MST009 Mastocytosis 56 0.043
141
DBT010 Diabetic Neuropathy 55 0.043
142
P TMT001 Timothy Syndrome 55 0.043
143
P FNC043 Fanconi Anemia, Complementation Group E 55 0.043
144
P LPR002 Leopard Syndrome 55 0.043
145
SML033 Small Cell Cancer of the Lung, Somatic 54 0.043
146
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.043
147
LYM040 Lymphoblastic Lymphoma 53 0.043
148
GNG012 Gingival Overgrowth 52 0.043
149
KRT009 Keratosis 52 0.043
150
PRS042 Prostate Disease 52 0.043
151
c LNG050 Long Qt Syndrome 5 51 0.043
152
CRY005 Cryptococcosis 50 0.043
153
P LFT003 Left Ventricular Noncompaction 50 0.043
154
BNF002 Bone Fracture 50 0.043
155
P PRX021 Proximal Symphalangism 50 0.043
156
P CLL015 Collagen Disease 50 0.043
157
c LNG051 Long Qt Syndrome 6 49 0.043
158
ERY017 Erythema Elevatum Diutinum 49 0.043
159
ATR057 Atrioventricular Block 49 0.043
160
c LNG092 Long Qt Syndrome-3 49 0.043
161
LPD004 Lipoid Nephrosis 48 0.043
162
FSC004 Fasciitis 48 0.043
163
LYM008 Lymphangiosarcoma 47 0.043
164
P TCL004 T-Cell Leukemia 47 0.043
165
NTR003 Natural Killer Cell Leukemia 47 0.043
166
SDD007 Sudden Cardiac Death 47 0.043
167
SYN036 Syncope 47 0.043
168
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.043
169
PRP082 Porphyria, Congenital Erythropoietic 46 0.043
170
PTY003 Pityriasis Rubra Pilaris 46 0.043
171
c LNG056 Long Qt Syndrome 12 45 0.043
172
FBR009 Fibrous Dysplasia 45 0.043
173
c SHR030 Short Qt Syndrome 44 0.043
174
P NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 44 0.043
175
DYS018 Dysostosis 44 0.043
176
c LNG057 Long Qt Syndrome 13 44 0.043
177
c LNG053 Long Qt Syndrome 9 44 0.043
178
HYP077 Hypertrichosis 44 0.043
179
DSM003 Desmoid Disease, Hereditary 44 0.043
180
FBR019 Fibromatosis 43 0.043
181
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.043
182
MTR003 Mitral Valve Stenosis 43 0.043
183
END072 Endotheliitis 42 0.043
184
c FML191 Familial Long Qt Syndrome 42 0.043
185
HRT008 Heart Conduction Disease 42 0.043
186
RHM014 Rheumatoid Vasculitis 42 0.043
187
AGG002 Aggressive Systemic Mastocytosis 42 0.043
188
AND010 Androgen Insensitivity, Partial, with or Without Breast Cancer 42 0.043
189
EXS001 Exostosis 42 0.043
190
P PRM018 Primary Hypertrophic Osteoarthropathy 42 0.043
191
RTR008 Root Resorption 42 0.043
192
VNT011 Ventricular Fibrillation, Familial, 1 41 0.043
193
PHC013 Phaeochromocytoma 41 0.043
194
PRD003 Periodontosis 41 0.043
195
ANH002 Anhidrosis 41 0.043
196
BNG036 Bone Giant Cell Tumor 41 0.043
197
MDS022 Mediastinitis 41 0.043
198
ACT055 Actinomycosis 40 0.043
199
BND014 Bone Development Disease 40 0.043
200
TND005 Tendinitis 39 0.043
201
MLR003 Melorheostosis 39 0.043
202
c PRS116 Prostate Cancer 1 37 0.043
203
FRY002 Fryns Syndrome 37 0.043
204
BNS002 Bone Structure Disease 37 0.043
205
P PST059 Pustular Psoriasis 36 0.043
206
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.043
207
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 35 0.043
208
GNT005 Giant Hemangioma 35 0.043
209
ADP007 Adie Pupil 34 0.043
210
CRB079 Cerebrospinal Fluid Leak 34 0.043
211
FRN039 Frank-Ter Haar Syndrome 34 0.043
212
ACR002 Acrocapitofemoral Dysplasia 33 0.043
213
LTR009 Lateral Meningocele Syndrome 31 0.043
214
c FRN011 Frontal Sinusitis 31 0.043
215
PRM243 Primary Bone Cancer 29 0.043
216
c MLT126 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1 28 0.043
217
c SCL052 Scleroderma, Familial Progressive 27 0.043
218
CLC004 Calcific Tendinitis 27 0.043
219
c FML294 Familial Short Qt Syndrome 26 0.043
220
P MLT140 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 26 0.043
221
MNN002 Mononeuritis Multiplex 25 0.043
222
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 24 0.043
223
c CHR040 Chronic Frontal Sinusitis 24 0.043
224
PGT009 Paget Disease of Bone 2, Early-Onset 20 0.043
225
MNS012 Monostotic Fibrous Dysplasia 20 0.043
226
c SNG012 Singleton-Merten Syndrome 2 13 0.043
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