Search results for "osteolysis"

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

176 hits were found for 'osteolysis'

# Family MCID Name MIFTS Score
1
TRG005 Torg Winchester Syndrome 51 6.386
2
GRH001 Gorham's Disease 32 5.695
3
PLY045 Polyostotic Osteolytic Dysplasia, Hereditary Expansile 22 5.200
4
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 20 4.436
5
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 12 4.381
6
PTT018 Petit-Fryns Syndrome 13 3.940
7
TLP005 Talo-Patello-Scaphoid Osteolysis 12 3.441
8
MLT033 Multicentric Osteolysis Nephropathy 6 3.441
9
OST045 Osteolysis Syndrome Recessive 4 3.393
10
CRP008 Carpo Tarsal Osteolysis Recessive 2 2.800
11
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 2 2.800
12
MLT064 Multicentric Osteolysis of Torg 6 2.771
13
VNB002 Van Bogaert-Hozay Syndrome 5 2.771
14
PHL009 Phalangeal Microgeodic Syndrome 11 1.998
15
NST002 Nestor-Guillermo Progeria Syndrome 20 1.959
16
PNT007 Penttinen-Aula Syndrome 7 1.959
17
HJD001 Hajdu-Cheney Syndrome 50 0.162
18
P BRS047 Breast Cancer 100 0.141
19
P ART022 Arthritis 75 0.133
20
c MYL007 Myeloma 61 0.124
21
P PRS040 Prostate Cancer 87 0.094
22
P MLT019 Multiple Myeloma 82 0.094
23
P OST002 Osteoporosis 75 0.094
24
PRG004 Progeria 72 0.094
25
PRS047 Prostatitis 60 0.094
26
P SYN007 Synovitis 59 0.094
27
ANG037 Angiomatosis 38 0.094
28
P SYS005 Systemic Scleroderma 66 0.081
29
HYP004 Hypercalcemia 65 0.081
30
c SCL016 Scleroderma 64 0.081
31
P ART023 Arthropathy 63 0.081
32
MND007 Mandibuloacral Dysplasia 60 0.081
33
P CRV039 Cervicitis 57 0.081
34
P RHM011 Rheumatoid Arthritis 93 0.066
35
P OST018 Osteosarcoma 79 0.066
36
P HMN010 Hemangioma 70 0.066
37
SRC014 Sarcoma 69 0.066
38
DSM004 Desmoid Tumor 67 0.066
39
P SYS004 Systemic Mastocytosis 66 0.066
40
P PRD008 Periodontitis 66 0.066
41
VSC011 Vasculitis 66 0.066
42
OLL001 Ollier Disease 66 0.066
43
P EPN002 Ependymoma 62 0.066
44
PYC001 Pycnodysostosis 62 0.066
45
SCN006 Secondary Syphilis 57 0.066
46
LNG024 Langerhans-Cell Histiocytosis 56 0.066
47
LYM019 Lymphosarcoma 54 0.066
48
MNT147 Mental Retardation 51 0.066
49
MYX001 Myxopapillary Ependymoma 49 0.066
50
SCH016 Schimke Immunoosseous Dysplasia 46 0.066
51
KRT012 Keratoderma 45 0.066
52
TTR016 Tetra-Amelia Syndrome 41 0.066
53
c HYP087 Hypotrichosis 41 0.066
54
LYM095 Lymphangiomatosis 37 0.066
55
P MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 32 0.066
56
HDG007 Hodgkin's Lymphoma 92 0.047
57
P HYP075 Hypertension 85 0.047
58
P PRM021 Primary Pulmonary Hypertension 82 0.047
59
P GCH001 Gaucher's Disease 77 0.047
60
P LKM002 Leukemia 77 0.047
61
SKN016 Skin Disease 75 0.047
62
P LPR002 Leopard Syndrome 73 0.047
63
c PRM002 Primary Hyperoxaluria 72 0.047
64
c MST009 Mastocytosis 71 0.047
65
RLP001 Relapsing Polychondritis 70 0.047
66
c THR014 Thrombocytopenia 70 0.047
67
PLY017 Polyarteritis Nodosa 69 0.047
68
ACN002 Acanthosis Nigricans 69 0.047
69
CRY005 Cryptococcosis 68 0.047
70
ERD001 Erdheim-Chester Disease 66 0.047
71
c JVN010 Juvenile Rheumatoid Arthritis 65 0.047
72
P SHR002 Short Stature 64 0.047
73
FLT001 Felty's Syndrome 63 0.047
74
c EHL001 Ehlers-Danlos Syndrome 63 0.047
75
MXD005 Mixed Connective Tissue Disease 63 0.047
76
P OST001 Osteopetrosis 63 0.047
77
OCC006 Occipital Horn Syndrome 62 0.047
78
PRT092 Partial Androgen Insensitivity Syndrome 62 0.047
79
GNG013 Gingivitis 62 0.047
80
NRP001 Neuropathy 61 0.047
81
DBT010 Diabetic Neuropathy 60 0.047
82
P DFF005 Diffuse Large B-Cell Lymphoma 60 0.047
83
c AGM001 Agammaglobulinemia 60 0.047
84
LPD010 Lipodystrophy 59 0.047
85
SPH001 Sapho Syndrome 59 0.047
86
c LCL006 Localized Scleroderma 59 0.047
87
MYC002 Mycobacterium Avium Complex Disease 58 0.047
88
CNN005 Connective Tissue Disease 58 0.047
89
PRT039 Proteinuria 57 0.047
90
P GNT008 Giant Cell Tumor 57 0.047
91
P SNS014 Sinusitis 57 0.047
92
KDS001 Kid Syndrome 57 0.047
93
RLY001 Riley-Day Syndrome 57 0.047
94
CNG402 Congenital Insensitivity to Pain with Anhidrosis 57 0.047
95
ANK001 Ankylosis 57 0.047
96
DFF003 Diffuse Scleroderma 56 0.047
97
P EXP004 Exophthalmos 54 0.047
98
PLY012 Polyhydramnios 54 0.047
99
ANH002 Anhidrosis 54 0.047
100
LYM040 Lymphoblastic Lymphoma 54 0.047
101
P EHL009 Ehlers-Danlos Syndrome Type Iv 53 0.047
102
AGG002 Aggressive Systemic Mastocytosis 52 0.047
103
GNG012 Gingival Overgrowth 51 0.047
104
VHW001 Vohwinkel Syndrome 51 0.047
105
EXS001 Exostosis 51 0.047
106
CLC006 Calcinosis 51 0.047
107
MNN014 Mononeuritis 51 0.047
108
END072 Endotheliitis 50 0.047
109
c TCL004 T-Cell Leukemia 50 0.047
110
c INT191 Intestinal Lymphangiectasia 50 0.047
111
FBR009 Fibrous Dysplasia 50 0.047
112
BLC003 Bloch-Sulzberger Syndrome 50 0.047
113
ERY017 Erythema Elevatum Diutinum 49 0.047
114
KRT009 Keratosis 49 0.047
115
P SPN052 Spondyloarthropathy 49 0.047
116
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 49 0.047
117
CHR288 Chronic Recurrent Multifocal Osteomyelitis 49 0.047
118
P BCL006 B-Cell Lymphomas 49 0.047
119
RHM014 Rheumatoid Vasculitis 48 0.047
120
LYM008 Lymphangiosarcoma 47 0.047
121
FBR019 Fibromatosis 47 0.047
122
ACT055 Actinomycosis 46 0.047
123
PTY003 Pityriasis Rubra Pilaris 46 0.047
124
EVN001 Evans' Syndrome 46 0.047
125
c ADL017 Adult T-Cell Leukemia 46 0.047
126
MDS022 Mediastinitis 46 0.047
127
DYS018 Dysostosis 45 0.047
128
FSC004 Fasciitis 45 0.047
129
TND005 Tendinitis 45 0.047
130
ANR040 Aneurysm 44 0.047
131
PPL006 Papillon-Lefevre Disease 44 0.047
132
CRN077 Cranio Osteoarthropathy 42 0.047
133
PHC013 Phaeochromocytoma 42 0.047
134
P ATX010 Ataxia Neuropathy Spectrum 41 0.047
135
MLR003 Melorheostosis 41 0.047
136
P HRD033 Hereditary Sensory and Autonomic Neuropathy Type Ii 40 0.047
137
GCH006 Gaucher Disease Perinatal Lethal 40 0.047
138
HMM002 Haim-Munk Syndrome 39 0.047
139
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 39 0.047
140
MNN002 Mononeuritis Multiplex 38 0.047
141
P EXS004 Exostoses, Multiple, Type 1 38 0.047
142
PLM029 Palmoplantar Keratosis 37 0.047
143
OLM001 Olmsted Syndrome 37 0.047
144
P GMM003 Gamma Heavy Chain Disease 37 0.047
145
c GCH005 Gaucher Disease Type 3 37 0.047
146
RTR008 Root Resorption 36 0.047
147
ORL015 Oral Squamous Cell Carcinoma 36 0.047
148
ENC010 Encephalocraniocutaneous Lipomatosis 35 0.047
149
HYL002 Hyalinosis, Inherited Systemic 35 0.047
150
P MYF007 Myofibromatosis, Infantile, 1 35 0.047
151
ADS002 Adie Syndrome 35 0.047
152
P KRT056 Keratosis Palmoplantaris Striata I, Ad 34 0.047
153
KLD001 Keloids 34 0.047
154
SYN053 Syndromic Diarrhea 32 0.047
155
ZNC001 Zunich Neuroectodermal Syndrome 31 0.047
156
P ATS061 Autosomal Recessive Hypotrichosis 31 0.047
157
CRB079 Cerebrospinal Fluid Leak 30 0.047
158
c FRN011 Frontal Sinusitis 30 0.047
159
MLD003 Meleda Disease 29 0.047
160
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 29 0.047
161
RCK007 Rickets, Vitamin D-Resistant, Type Iia 29 0.047
162
GNT005 Giant Hemangioma 27 0.047
163
HNM002 Hinman Syndrome 27 0.047
164
XNT009 Xanthoma Disseminatum 27 0.047
165
CLC004 Calcific Tendinitis 26 0.047
166
RMN002 Ramon Syndrome 26 0.047
167
MNS012 Monostotic Fibrous Dysplasia 24 0.047
168
HSH001 Hashimoto-Pritzker Syndrome 22 0.047
169
c BNG076 Benign Exophthalmos Syndrome 22 0.047
170
PRD003 Periodontosis 21 0.047
171
AND005 Androgen Insensitivity Syndrome, Mild 21 0.047
172
INT238 Intellectual Disability - Cataracts - Calcified Pinnae - Myopathy 18 0.047
173
c CHR040 Chronic Frontal Sinusitis 18 0.047
174
DRM020 Dermatoosteolysis Kirghizian Type 17 0.047
175
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 17 0.047
176
CMP053 Camptodactyly of Fingers 16 0.047