Search results for "osteolysis"

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

183 hits were found for 'osteolysis'

# Family MCID Name MIFTS Score
1
TRG005 Torg Winchester Syndrome 52 7.181
2
GRH001 Gorham's Disease 32 5.630
3
PLY045 Polyostotic Osteolytic Dysplasia, Hereditary Expansile 24 5.141
4
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 20 4.795
5
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 12 4.331
6
PTT018 Petit-Fryns Syndrome 13 3.895
7
ATS198 Autosomal Recessive Carpotarsal Osteolysis 4 3.873
8
TLP005 Talo-Patello-Scaphoid Osteolysis 12 3.401
9
MLT033 Multicentric Osteolysis Nephropathy 5 3.401
10
VNB002 Van Bogaert-Hozay Syndrome 5 3.354
11
OST045 Osteolysis Syndrome Recessive 4 3.354
12
CRP008 Carpo Tarsal Osteolysis Recessive 2 2.768
13
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 2 2.768
14
MLT064 Multicentric Osteolysis of Torg 5 2.739
15
PHL009 Phalangeal Microgeodic Syndrome 11 1.975
16
NST002 Nestor-Guillermo Progeria Syndrome 20 1.937
17
PNT007 Penttinen-Aula Syndrome 8 1.937
18
HJD001 Hajdu-Cheney Syndrome 50 0.174
19
P BRS047 Breast Cancer 86 0.147
20
P ART022 Arthritis 75 0.139
21
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.131
22
c MYL007 Myeloma 61 0.123
23
P PRS040 Prostate Cancer 98 0.093
24
P MLT019 Multiple Myeloma 88 0.093
25
P GCH001 Gaucher's Disease 84 0.093
26
P OST002 Osteoporosis 76 0.093
27
PRG004 Progeria 73 0.093
28
P SYS005 Systemic Scleroderma 66 0.093
29
P ART023 Arthropathy 64 0.093
30
PRS047 Prostatitis 60 0.093
31
P SYN007 Synovitis 60 0.093
32
LNG024 Langerhans-Cell Histiocytosis 57 0.093
33
ANG037 Angiomatosis 38 0.093
34
c SCL016 Scleroderma 65 0.080
35
HYP004 Hypercalcemia 65 0.080
36
MND007 Mandibuloacral Dysplasia 61 0.080
37
P CRV039 Cervicitis 58 0.080
38
SCH016 Schimke Immunoosseous Dysplasia 47 0.080
39
TTR016 Tetra-Amelia Syndrome 42 0.080
40
P RHM011 Rheumatoid Arthritis 94 0.066
41
P OST018 Osteosarcoma 82 0.066
42
CYS008 Cystic Echinococcosis 74 0.066
43
RLP001 Relapsing Polychondritis 72 0.066
44
P HMN010 Hemangioma 71 0.066
45
SRC014 Sarcoma 70 0.066
46
NVD001 Nevoid Basal Cell Carcinoma Syndrome 69 0.066
47
DSM004 Desmoid Tumor 69 0.066
48
P PRD008 Periodontitis 67 0.066
49
OLL001 Ollier Disease 66 0.066
50
VSC011 Vasculitis 66 0.066
51
PYC001 Pycnodysostosis 62 0.066
52
P EPN002 Ependymoma 62 0.066
53
SPH001 Sapho Syndrome 60 0.066
54
c SYS004 Systemic Mastocytosis 59 0.066
55
LYM019 Lymphosarcoma 59 0.066
56
P GNT008 Giant Cell Tumor 58 0.066
57
SCN006 Secondary Syphilis 57 0.066
58
DFF003 Diffuse Scleroderma 57 0.066
59
MNT147 Mental Retardation 52 0.066
60
MNN014 Mononeuritis 51 0.066
61
MYX001 Myxopapillary Ependymoma 50 0.066
62
KRT012 Keratoderma 46 0.066
63
c HYP087 Hypotrichosis 42 0.066
64
LYM095 Lymphangiomatosis 38 0.066
65
P MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 0.066
66
KLD001 Keloids 34 0.066
67
HDG007 Hodgkin's Lymphoma 93 0.046
68
P HYP075 Hypertension 87 0.046
69
P LKM002 Leukemia 77 0.046
70
P PRM021 Primary Pulmonary Hypertension 77 0.046
71
SKN016 Skin Disease 75 0.046
72
P LPR002 Leopard Syndrome 75 0.046
73
P MST009 Mastocytosis 75 0.046
74
c PRM002 Primary Hyperoxaluria 74 0.046
75
c PLM037 Pulmonary Hypertension 73 0.046
76
c THR014 Thrombocytopenia 71 0.046
77
PLY017 Polyarteritis Nodosa 69 0.046
78
ALV002 Alveolar Echinococcosis 68 0.046
79
CRY005 Cryptococcosis 68 0.046
80
P SHR002 Short Stature 68 0.046
81
ERD001 Erdheim-Chester Disease 67 0.046
82
c JVN010 Juvenile Rheumatoid Arthritis 66 0.046
83
P OST001 Osteopetrosis 66 0.046
84
c EHL001 Ehlers-Danlos Syndrome 64 0.046
85
FLT001 Felty's Syndrome 64 0.046
86
MXD005 Mixed Connective Tissue Disease 64 0.046
87
ACN002 Acanthosis Nigricans 63 0.046
88
PRT092 Partial Androgen Insensitivity Syndrome 62 0.046
89
OCC006 Occipital Horn Syndrome 62 0.046
90
NRP001 Neuropathy 62 0.046
91
GNG013 Gingivitis 61 0.046
92
DBT010 Diabetic Neuropathy 61 0.046
93
c AGM001 Agammaglobulinemia 61 0.046
94
CNG402 Congenital Insensitivity to Pain with Anhidrosis 59 0.046
95
c LCL006 Localized Scleroderma 59 0.046
96
MYC002 Mycobacterium Avium Complex Disease 59 0.046
97
LPD010 Lipodystrophy 59 0.046
98
CNN005 Connective Tissue Disease 58 0.046
99
PRT039 Proteinuria 58 0.046
100
P SNS014 Sinusitis 58 0.046
101
KDS001 Kid Syndrome 58 0.046
102
RLY001 Riley-Day Syndrome 58 0.046
103
ANK001 Ankylosis 57 0.046
104
P BCL006 B-Cell Lymphomas 57 0.046
105
DFF005 Diffuse Large B-Cell Lymphoma 56 0.046
106
P EXP004 Exophthalmos 55 0.046
107
INC001 Incontinentia Pigmenti Achromians 55 0.046
108
PLY012 Polyhydramnios 54 0.046
109
ANH002 Anhidrosis 54 0.046
110
LYM040 Lymphoblastic Lymphoma 54 0.046
111
P EHL009 Ehlers-Danlos Syndrome Type Iv 53 0.046
112
CLC006 Calcinosis 53 0.046
113
AGG002 Aggressive Systemic Mastocytosis 52 0.046
114
GNG012 Gingival Overgrowth 52 0.046
115
VHW001 Vohwinkel Syndrome 52 0.046
116
EXS001 Exostosis 52 0.046
117
JNT002 Joint Disorders 51 0.046
118
END072 Endotheliitis 51 0.046
119
FBR009 Fibrous Dysplasia 51 0.046
120
c TCL004 T-Cell Leukemia 51 0.046
121
KRT009 Keratosis 50 0.046
122
ERY017 Erythema Elevatum Diutinum 50 0.046
123
CHR288 Chronic Recurrent Multifocal Osteomyelitis 50 0.046
124
RHM014 Rheumatoid Vasculitis 49 0.046
125
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 49 0.046
126
LYM008 Lymphangiosarcoma 48 0.046
127
ACT055 Actinomycosis 47 0.046
128
PTY003 Pityriasis Rubra Pilaris 47 0.046
129
FBR019 Fibromatosis 47 0.046
130
c ADL017 Adult T-Cell Leukemia 46 0.046
131
MDS022 Mediastinitis 46 0.046
132
ANR040 Aneurysm 46 0.046
133
EVN001 Evans' Syndrome 46 0.046
134
DYS018 Dysostosis 46 0.046
135
FSC004 Fasciitis 46 0.046
136
P SPN052 Spondyloarthropathy 46 0.046
137
TND005 Tendinitis 45 0.046
138
P PRX021 Proximal Symphalangism 45 0.046
139
PPL006 Papillon-Lefevre Disease 44 0.046
140
P HRD033 Hereditary Sensory and Autonomic Neuropathy Type Ii 44 0.046
141
P ATX010 Ataxia Neuropathy Spectrum 43 0.046
142
PHC013 Phaeochromocytoma 43 0.046
143
CRN077 Cranio Osteoarthropathy 43 0.046
144
MLR003 Melorheostosis 41 0.046
145
HMM002 Haim-Munk Syndrome 40 0.046
146
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 39 0.046
147
P EXS004 Exostoses, Multiple, Type 1 39 0.046
148
MNN002 Mononeuritis Multiplex 38 0.046
149
ORL015 Oral Squamous Cell Carcinoma 38 0.046
150
PLM029 Palmoplantar Keratosis 38 0.046
151
c GCH005 Gaucher Disease Type 3 38 0.046
152
P GMM003 Gamma Heavy Chain Disease 37 0.046
153
RTR008 Root Resorption 36 0.046
154
ADS002 Adie Syndrome 35 0.046
155
ENC010 Encephalocraniocutaneous Lipomatosis 35 0.046
156
HYL002 Hyalinosis, Inherited Systemic 35 0.046
157
P KRT056 Keratosis Palmoplantaris Striata I, Ad 35 0.046
158
P MYF007 Myofibromatosis, Infantile, 1 35 0.046
159
SYN053 Syndromic Diarrhea 34 0.046
160
P ATS061 Autosomal Recessive Hypotrichosis 33 0.046
161
ZNC001 Zunich Neuroectodermal Syndrome 31 0.046
162
CRB079 Cerebrospinal Fluid Leak 30 0.046
163
c FRN011 Frontal Sinusitis 30 0.046
164
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 30 0.046
165
TRL002 Tarlov Cysts 29 0.046
166
MLD003 Meleda Disease 29 0.046
167
RCK007 Rickets, Vitamin D-Resistant, Type Iia 28 0.046
168
HNM002 Hinman Syndrome 28 0.046
169
OLM002 Olmsted Syndrome, X-Linked 28 0.046
170
GNT005 Giant Hemangioma 28 0.046
171
CLC004 Calcific Tendinitis 27 0.046
172
XNT009 Xanthoma Disseminatum 26 0.046
173
RMN002 Ramon Syndrome 26 0.046
174
PRM056 Primrose Syndrome 25 0.046
175
MNS012 Monostotic Fibrous Dysplasia 24 0.046
176
c BNG076 Benign Exophthalmos Syndrome 22 0.046
177
HSH001 Hashimoto-Pritzker Syndrome 22 0.046
178
PRD003 Periodontosis 22 0.046
179
AND005 Androgen Insensitivity Syndrome, Mild 21 0.046
180
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 18 0.046
181
DRM020 Dermatoosteolysis Kirghizian Type 18 0.046
182
c CHR040 Chronic Frontal Sinusitis 17 0.046
183
CMP053 Camptodactyly of Fingers 16 0.046