Search results for "osteolysis"

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

197 hits were found for 'osteolysis'

# Family MCID Name MIFTS Score
1
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 42 8.107
2
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 50 7.837
3
OST079 Osteolysis, Familial Expansile 39 6.095
4
CYS041 Cystic Angiomatosis of Bone, Diffuse 35 5.083
5
OST149 Osteolysis Syndrome, Recessive 16 4.340
6
MLT033 Multicentric Osteolysis Nephropathy 11 3.925
7
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 10 3.847
8
HJD001 Hajdu-Cheney Syndrome 58 3.543
9
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 12 3.453
10
NST002 Nestor-Guillermo Progeria Syndrome 22 3.342
11
MLT064 Multicentric Osteolysis of Torg 6 1.993
12
IDP078 Idiopathic Phalangeal Acro-Osteolysis 5 1.993
13
CRP008 Carpo Tarsal Osteolysis Recessive 2 1.993
14
c MLT138 Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum 7 1.969
15
PHL009 Phalangeal Microgeodic Syndrome 9 1.941
16
PTT018 Petit-Fryns Syndrome 4 1.941
17
VNB002 Van Bogaert-Hozay Syndrome 7 1.904
18
PNT007 Penttinen-Aula Syndrome 6 1.904
19
P BRS047 Breast Cancer 100 0.162
20
P ART023 Arthropathy 63 0.149
21
WNC001 Winchester Syndrome 39 0.149
22
P ART022 Arthritis 75 0.127
23
P PRS040 Prostate Cancer 89 0.119
24
P OST002 Osteoporosis 64 0.110
25
P MLT019 Multiple Myeloma 80 0.101
26
PRS047 Prostatitis 56 0.101
27
MND007 Mandibuloacral Dysplasia 49 0.101
28
P GNT008 Giant Cell Tumor 49 0.101
29
c GCH015 Gaucher Disease, Type I 66 0.090
30
CLC006 Calcinosis 49 0.090
31
ANG037 Angiomatosis 34 0.090
32
P LYM118 Lymphoma 70 0.078
33
HTC002 Hutchinson-Gilford Progeria 62 0.078
34
PYC001 Pycnodysostosis 49 0.078
35
P CRV039 Cervicitis 44 0.078
36
SYN007 Synovitis 41 0.078
37
HYL004 Hyaline Fibromatosis Syndrome 39 0.078
38
LYM095 Lymphangiomatosis 33 0.078
39
DRM042 Dermatoosteolysis, Kirghizian Type 15 0.078
40
P LNG032 Lung Cancer 94 0.064
41
SRC014 Sarcoma 66 0.064
42
P AGM001 Agammaglobulinemia 64 0.064
43
VSC011 Vasculitis 62 0.064
44
P HMN010 Hemangioma 60 0.064
45
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.064
46
INC021 Incontinentia Pigmenti 60 0.064
47
MSS002 Mass Syndrome 59 0.064
48
c SYS004 Systemic Mastocytosis 59 0.064
49
P SYS005 Systemic Scleroderma 58 0.064
50
JNT002 Joint Disorders 56 0.064
51
P HST010 Histiocytosis 55 0.064
52
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.064
53
P INT063 Intellectual Disability 53 0.064
54
LYM019 Lymphosarcoma 53 0.064
55
P EPN002 Ependymoma 53 0.064
56
KDS001 Kid Syndrome 53 0.064
57
ERD001 Erdheim-Chester Disease 51 0.064
58
HPT074 Hepatic Adenoma, Somatic 51 0.064
59
KLD001 Keloids 51 0.064
60
c EHL055 Ehlers-Danlos Syndrome, Type Iii 50 0.064
61
c DYS166 Dysautonomia, Familial 50 0.064
62
PPL049 Papillon-Lefevre Syndrome 46 0.064
63
P PRD008 Periodontitis 46 0.064
64
c GMM003 Gamma Heavy Chain Disease 45 0.064
65
P INF049 Infantile Myofibromatosis 45 0.064
66
BNC003 Bone Cancer 45 0.064
67
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.064
68
FLT011 Felty Syndrome 45 0.064
69
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.064
70
P HYP087 Hypotrichosis 45 0.064
71
c GCH017 Gaucher Disease, Type Iii 45 0.064
72
SPH001 Sapho Syndrome 44 0.064
73
DSM003 Desmoid Disease, Hereditary 44 0.064
74
ENC044 Enchondromatosis, Multiple, Ollier Type 44 0.064
75
c NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 43 0.064
76
c HRD104 Hereditary Multiple Osteochondromas 43 0.064
77
P MSC022 Mosaic Variegated Aneuploidy Syndrome 42 0.064
78
VHW001 Vohwinkel Syndrome 41 0.064
79
MYX001 Myxopapillary Ependymoma 40 0.064
80
MLT145 Multiple Enchondromatosis, Maffucci Type 40 0.064
81
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.064
82
RCK007 Rickets, Vitamin D-Resistant, Type Iia 37 0.064
83
ALR002 Al-Raqad Syndrome 36 0.064
84
TTR016 Tetra-Amelia Syndrome 36 0.064
85
ACR005 Acrodermatitis 34 0.064
86
XNT009 Xanthoma Disseminatum 33 0.064
87
PRM056 Primrose Syndrome 32 0.064
88
RMN002 Ramon Syndrome 31 0.064
89
TRL002 Tarlov Cysts 29 0.064
90
c SCL052 Scleroderma, Familial Progressive 27 0.064
91
HNM002 Hinman Syndrome 25 0.064
92
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 24 0.064
93
BNR002 Bone Resorption Disease 22 0.064
94
PRM206 Premature Aging Syndrome, Penttinen Type 21 0.064
95
c SNG011 Singleton-Merten Syndrome 1 18 0.064
96
AND005 Androgen Insensitivity Syndrome, Mild 16 0.064
97
HSH001 Hashimoto-Pritzker Syndrome 16 0.064
98
P RHM011 Rheumatoid Arthritis 88 0.045
99
P OST012 Osteoarthritis 82 0.045
100
P PLM037 Pulmonary Hypertension 79 0.045
101
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.045
102
HDG012 Hodgkin Lymphoma 73 0.045
103
P LKM002 Leukemia 70 0.045
104
BSL036 Basal Cell Nevus Syndrome 65 0.045
105
P BCL006 B-Cell Lymphomas 64 0.045
106
EWN003 Ewing Sarcoma 64 0.045
107
P THR014 Thrombocytopenia 64 0.045
108
P PSR002 Psoriasis 63 0.045
109
P OST001 Osteopetrosis 62 0.045
110
P EHL001 Ehlers-Danlos Syndrome 61 0.045
111
CNN005 Connective Tissue Disease 61 0.045
112
GNG013 Gingivitis 60 0.045
113
P SPN052 Spondyloarthropathy 60 0.045
114
P SNS014 Sinusitis 60 0.045
115
P SHR029 Short Syndrome 60 0.045
116
P NRP001 Neuropathy 60 0.045
117
P RCK004 Rickets 59 0.045
118
c LCL006 Localized Scleroderma 59 0.045
119
ADM013 Adamantinoma of Long Bones 59 0.045
120
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 58 0.045
121
c ADL017 Adult T-Cell Leukemia 58 0.045
122
RHM027 Rheumatic Disease 57 0.045
123
ANR040 Aneurysm 57 0.045
124
DFF005 Diffuse Large B-Cell Lymphoma 56 0.045
125
ORL015 Oral Squamous Cell Carcinoma 56 0.045
126
DBT010 Diabetic Neuropathy 55 0.045
127
P PLY017 Polyarteritis Nodosa 55 0.045
128
LYM040 Lymphoblastic Lymphoma 54 0.045
129
P MST009 Mastocytosis 54 0.045
130
SML033 Small Cell Cancer of the Lung, Somatic 53 0.045
131
PRS042 Prostate Disease 52 0.045
132
HYP077 Hypertrichosis 52 0.045
133
GNG012 Gingival Overgrowth 52 0.045
134
ALV002 Alveolar Echinococcosis 51 0.045
135
DSM004 Desmoid Tumor 51 0.045
136
P HYP613 Hypophosphatemic Rickets 51 0.045
137
CRY005 Cryptococcosis 50 0.045
138
CYS008 Cystic Echinococcosis 50 0.045
139
KRT009 Keratosis 50 0.045
140
P CLL015 Collagen Disease 49 0.045
141
RLP001 Relapsing Polychondritis 49 0.045
142
LYM008 Lymphangiosarcoma 48 0.045
143
LPD004 Lipoid Nephrosis 48 0.045
144
BNF002 Bone Fracture 47 0.045
145
NTR003 Natural Killer Cell Leukemia 47 0.045
146
PTY003 Pityriasis Rubra Pilaris 46 0.045
147
OCC006 Occipital Horn Syndrome 46 0.045
148
P TCL004 T-Cell Leukemia 46 0.045
149
FSC004 Fasciitis 46 0.045
150
PRP082 Porphyria, Congenital Erythropoietic 46 0.045
151
DYS018 Dysostosis 44 0.045
152
FBR009 Fibrous Dysplasia 44 0.045
153
EXS001 Exostosis 44 0.045
154
TND005 Tendinitis 43 0.045
155
RHM014 Rheumatoid Vasculitis 43 0.045
156
AGG002 Aggressive Systemic Mastocytosis 42 0.045
157
BNG036 Bone Giant Cell Tumor 42 0.045
158
ANH002 Anhidrosis 42 0.045
159
END072 Endotheliitis 42 0.045
160
FBR019 Fibromatosis 42 0.045
161
AND010 Androgen Insensitivity, Partial, with or Without Breast Cancer 42 0.045
162
BND014 Bone Development Disease 42 0.045
163
MDS022 Mediastinitis 41 0.045
164
RTR008 Root Resorption 41 0.045
165
ACT055 Actinomycosis 41 0.045
166
PRD003 Periodontosis 41 0.045
167
PHC013 Phaeochromocytoma 41 0.045
168
c PRS116 Prostate Cancer 1 41 0.045
169
ERY017 Erythema Elevatum Diutinum 39 0.045
170
P PRM018 Primary Hypertrophic Osteoarthropathy 39 0.045
171
RSD004 Rosai-Dorfman Disease 39 0.045
172
MLR003 Melorheostosis 38 0.045
173
BNS002 Bone Structure Disease 36 0.045
174
FRY002 Fryns Syndrome 36 0.045
175
CRB079 Cerebrospinal Fluid Leak 36 0.045
176
ACR002 Acrocapitofemoral Dysplasia 36 0.045
177
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 35 0.045
178
P PST059 Pustular Psoriasis 35 0.045
179
ESN017 Eosinophilic Granuloma 34 0.045
180
ADP007 Adie Pupil 34 0.045
181
ENC010 Encephalocraniocutaneous Lipomatosis 34 0.045
182
FRN039 Frank-Ter Haar Syndrome 34 0.045
183
OLM001 Olmsted Syndrome 33 0.045
184
CHM006 Chime Syndrome 33 0.045
185
GNT005 Giant Hemangioma 33 0.045
186
LTR009 Lateral Meningocele Syndrome 31 0.045
187
CLC004 Calcific Tendinitis 31 0.045
188
HMM002 Haim-Munk Syndrome 31 0.045
189
c FRN011 Frontal Sinusitis 30 0.045
190
MLD003 Meleda Disease 26 0.045
191
MNN002 Mononeuritis Multiplex 25 0.045
192
c CHR040 Chronic Frontal Sinusitis 23 0.045
193
MNS012 Monostotic Fibrous Dysplasia 20 0.045
194
PGT009 Paget Disease of Bone 2, Early-Onset 20 0.045
195
P DFN296 Deafness-Onychodystrophy Syndrome 16 0.045
196
c SNG012 Singleton-Merten Syndrome 2 14 0.045
197
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 12 0.045