Search results for "osteolysis"

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

185 hits were found for 'osteolysis'

# Family MCID Name MIFTS Score
1
TRG005 Torg Winchester Syndrome 53 7.218
2
GRH001 Gorham's Disease 32 5.629
3
PLY045 Polyostotic Osteolytic Dysplasia, Hereditary Expansile 25 5.140
4
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 21 4.863
5
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 12 4.330
6
PTT018 Petit-Fryns Syndrome 15 3.949
7
ATS198 Autosomal Recessive Carpotarsal Osteolysis 4 3.873
8
TLP005 Talo-Patello-Scaphoid Osteolysis 13 3.471
9
MLT033 Multicentric Osteolysis Nephropathy 5 3.400
10
VNB002 Van Bogaert-Hozay Syndrome 9 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 2.738
15
PHL009 Phalangeal Microgeodic Syndrome 11 1.975
16
NST002 Nestor-Guillermo Progeria Syndrome 24 1.936
17
PNT007 Penttinen-Aula Syndrome 8 1.936
18
HJD001 Hajdu-Cheney Syndrome 51 0.173
19
P BRS047 Breast Cancer 85 0.146
20
P ART022 Arthritis 74 0.139
21
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.131
22
c MYL007 Myeloma 60 0.122
23
PRG004 Progeria 73 0.103
24
P PRS040 Prostate Cancer 97 0.092
25
P MLT019 Multiple Myeloma 88 0.092
26
P GCH001 Gaucher's Disease 83 0.092
27
P OST002 Osteoporosis 76 0.092
28
P SYS005 Systemic Scleroderma 66 0.092
29
OLL001 Ollier Disease 66 0.092
30
P ART023 Arthropathy 63 0.092
31
MND007 Mandibuloacral Dysplasia 62 0.092
32
PRS047 Prostatitis 59 0.092
33
P SYN007 Synovitis 59 0.092
34
LNG024 Langerhans-Cell Histiocytosis 57 0.092
35
P MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 38 0.092
36
ANG037 Angiomatosis 38 0.092
37
DSM004 Desmoid Tumor 68 0.080
38
c SCL016 Scleroderma 64 0.080
39
HYP004 Hypercalcemia 64 0.080
40
PYC001 Pycnodysostosis 63 0.080
41
P CRV039 Cervicitis 57 0.080
42
SCH016 Schimke Immunoosseous Dysplasia 48 0.080
43
TTR016 Tetra-Amelia Syndrome 43 0.080
44
HYL002 Hyalinosis, Inherited Systemic 35 0.080
45
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 19 0.080
46
DRM020 Dermatoosteolysis Kirghizian Type 19 0.080
47
P RHM011 Rheumatoid Arthritis 94 0.065
48
HDG007 Hodgkin's Lymphoma 93 0.065
49
P OST018 Osteosarcoma 81 0.065
50
CYS008 Cystic Echinococcosis 73 0.065
51
RLP001 Relapsing Polychondritis 72 0.065
52
P HMN010 Hemangioma 70 0.065
53
NVD001 Nevoid Basal Cell Carcinoma Syndrome 69 0.065
54
PLY017 Polyarteritis Nodosa 69 0.065
55
SRC014 Sarcoma 68 0.065
56
ALV002 Alveolar Echinococcosis 68 0.065
57
P PRD008 Periodontitis 68 0.065
58
ERD001 Erdheim-Chester Disease 67 0.065
59
VSC011 Vasculitis 65 0.065
60
c SYS004 Systemic Mastocytosis 64 0.065
61
FLT001 Felty's Syndrome 64 0.065
62
MXD005 Mixed Connective Tissue Disease 64 0.065
63
OCC006 Occipital Horn Syndrome 63 0.065
64
P EPN002 Ependymoma 61 0.065
65
c AGM001 Agammaglobulinemia 61 0.065
66
SPH001 Sapho Syndrome 60 0.065
67
KDS001 Kid Syndrome 58 0.065
68
RLY001 Riley-Day Syndrome 58 0.065
69
LYM019 Lymphosarcoma 58 0.065
70
DFF003 Diffuse Scleroderma 57 0.065
71
P GNT008 Giant Cell Tumor 57 0.065
72
INC001 Incontinentia Pigmenti Achromians 56 0.065
73
SCN006 Secondary Syphilis 56 0.065
74
c MNT147 Mental Retardation 56 0.065
75
P EHL009 Ehlers-Danlos Syndrome Type Iv 53 0.065
76
VHW001 Vohwinkel Syndrome 52 0.065
77
MNN014 Mononeuritis 51 0.065
78
CHR288 Chronic Recurrent Multifocal Osteomyelitis 50 0.065
79
MYX001 Myxopapillary Ependymoma 49 0.065
80
P EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 49 0.065
81
KRT012 Keratoderma 45 0.065
82
PPL006 Papillon-Lefevre Disease 45 0.065
83
CRN077 Cranio Osteoarthropathy 43 0.065
84
P HRD033 Hereditary Sensory and Autonomic Neuropathy Type Ii 43 0.065
85
c HYP087 Hypotrichosis 42 0.065
86
HMM002 Haim-Munk Syndrome 40 0.065
87
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 40 0.065
88
P EXS004 Exostoses, Multiple, Type 1 39 0.065
89
c GCH005 Gaucher Disease Type 3 39 0.065
90
P GMM003 Gamma Heavy Chain Disease 37 0.065
91
LYM095 Lymphangiomatosis 37 0.065
92
ENC010 Encephalocraniocutaneous Lipomatosis 36 0.065
93
KLD001 Keloids 36 0.065
94
P MYF007 Myofibromatosis, Infantile, 1 35 0.065
95
ZNC001 Zunich Neuroectodermal Syndrome 32 0.065
96
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 31 0.065
97
TRL002 Tarlov Cysts 30 0.065
98
MLD003 Meleda Disease 30 0.065
99
RCK007 Rickets, Vitamin D-Resistant, Type Iia 29 0.065
100
OLM002 Olmsted Syndrome, X-Linked 28 0.065
101
PRM056 Primrose Syndrome 28 0.065
102
RMN002 Ramon Syndrome 27 0.065
103
XNT009 Xanthoma Disseminatum 27 0.065
104
HSH001 Hashimoto-Pritzker Syndrome 23 0.065
105
P HYP075 Hypertension 85 0.046
106
P PRM021 Primary Pulmonary Hypertension 80 0.046
107
PGT001 Paget's Disease of Bone 76 0.046
108
P LKM002 Leukemia 76 0.046
109
P MST009 Mastocytosis 75 0.046
110
P LPR002 Leopard Syndrome 75 0.046
111
c OST001 Osteopetrosis 75 0.046
112
SKN016 Skin Disease 74 0.046
113
c PLM037 Pulmonary Hypertension 73 0.046
114
c PRM002 Primary Hyperoxaluria 73 0.046
115
c THR014 Thrombocytopenia 69 0.046
116
P SHR002 Short Stature 68 0.046
117
CRY005 Cryptococcosis 67 0.046
118
c JVN010 Juvenile Rheumatoid Arthritis 67 0.046
119
ACN002 Acanthosis Nigricans 64 0.046
120
c EHL001 Ehlers-Danlos Syndrome 63 0.046
121
PRT092 Partial Androgen Insensitivity Syndrome 63 0.046
122
NRP001 Neuropathy 61 0.046
123
GNG013 Gingivitis 60 0.046
124
CNG402 Congenital Insensitivity to Pain with Anhidrosis 60 0.046
125
DBT010 Diabetic Neuropathy 60 0.046
126
c LCL006 Localized Scleroderma 59 0.046
127
MYC002 Mycobacterium Avium Complex Disease 58 0.046
128
LPD010 Lipodystrophy 58 0.046
129
CNN005 Connective Tissue Disease 58 0.046
130
PRT039 Proteinuria 57 0.046
131
P SNS014 Sinusitis 57 0.046
132
ANH002 Anhidrosis 57 0.046
133
ANK001 Ankylosis 56 0.046
134
P BCL006 B-Cell Lymphomas 56 0.046
135
DFF005 Diffuse Large B-Cell Lymphoma 55 0.046
136
P EXP004 Exophthalmos 54 0.046
137
PLY012 Polyhydramnios 54 0.046
138
LYM040 Lymphoblastic Lymphoma 53 0.046
139
AGG002 Aggressive Systemic Mastocytosis 52 0.046
140
CLC006 Calcinosis 52 0.046
141
P CNG119 Congenital Porphyria 52 0.046
142
JNT002 Joint Disorders 52 0.046
143
GNG012 Gingival Overgrowth 51 0.046
144
EXS001 Exostosis 51 0.046
145
END072 Endotheliitis 50 0.046
146
FBR009 Fibrous Dysplasia 50 0.046
147
c TCL004 T-Cell Leukemia 50 0.046
148
ERY017 Erythema Elevatum Diutinum 50 0.046
149
KRT009 Keratosis 49 0.046
150
RHM014 Rheumatoid Vasculitis 48 0.046
151
PTY003 Pityriasis Rubra Pilaris 47 0.046
152
LYM008 Lymphangiosarcoma 47 0.046
153
P ATX010 Ataxia Neuropathy Spectrum 47 0.046
154
ACT055 Actinomycosis 46 0.046
155
FBR019 Fibromatosis 46 0.046
156
c ADL017 Adult T-Cell Leukemia 45 0.046
157
P PRX021 Proximal Symphalangism 45 0.046
158
MDS022 Mediastinitis 45 0.046
159
ANR040 Aneurysm 45 0.046
160
EVN001 Evans' Syndrome 45 0.046
161
DYS018 Dysostosis 45 0.046
162
FSC004 Fasciitis 45 0.046
163
P SPN052 Spondyloarthropathy 45 0.046
164
TND005 Tendinitis 45 0.046
165
PHC013 Phaeochromocytoma 42 0.046
166
MLR003 Melorheostosis 40 0.046
167
MNN002 Mononeuritis Multiplex 38 0.046
168
ORL015 Oral Squamous Cell Carcinoma 38 0.046
169
PLM029 Palmoplantar Keratosis 38 0.046
170
c ATS061 Autosomal Recessive Hypotrichosis 36 0.046
171
RTR008 Root Resorption 36 0.046
172
P KRT056 Keratosis Palmoplantaris Striata I, Ad 35 0.046
173
ADS002 Adie Syndrome 35 0.046
174
SYN053 Syndromic Diarrhea 34 0.046
175
CRB079 Cerebrospinal Fluid Leak 30 0.046
176
c FRN011 Frontal Sinusitis 29 0.046
177
HNM002 Hinman Syndrome 28 0.046
178
GNT005 Giant Hemangioma 27 0.046
179
CLC004 Calcific Tendinitis 26 0.046
180
MNS012 Monostotic Fibrous Dysplasia 24 0.046
181
c BNG076 Benign Exophthalmos Syndrome 22 0.046
182
PRD003 Periodontosis 22 0.046
183
AND005 Androgen Insensitivity Syndrome, Mild 21 0.046
184
CMP053 Camptodactyly of Fingers 18 0.046
185
c CHR040 Chronic Frontal Sinusitis 16 0.046