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

194 hits were found for 'osteolysis'

# ++ Fam MCID Name MIFTS Score
1
TRG005 Torg Winchester Syndrome 39 6.130
2
GRH001 Gorham's Disease 25 5.493
3
PLY045 Polyostotic Osteolytic Dysplasia, Hereditary Expansile 16 4.730
4
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 12 4.372
5
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 8 4.338
6
PTT018 Petit-Fryns Syndrome 9 3.884
7
TLP005 Talo-Patello-Scaphoid Osteolysis 8 3.460
8
MLT033 Multicentric Osteolysis Nephropathy 5 3.410
9
ACR082 Acro-Osteolysis-Keloid-Like Lesions-Premature Aging Syndrome 8 3.345
10
OST045 Osteolysis Syndrome Recessive 1 3.345
11
CRP008 Carpo Tarsal Osteolysis Recessive 0 2.760
12
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 0 2.760
13
MLT064 Multicentric Osteolysis of Torg 4 2.731
14
PNT007 Penttinen-Aula Syndrome 4 1.969
15
NST002 Nestor-Guillermo Progeria Syndrome 10 1.931
16
PHL009 Phalangeal Microgeodic Syndrome 6 1.931
17
VNB002 Van Bogaert-Hozay Syndrome 2 1.931
18
HJD001 Hajdu-Cheney Syndrome 50 0.150
19
P BRS047 Breast Cancer 85 0.136
20
WNC001 Winchester Syndrome 29 0.136
21
P ART022 Arthritis 75 0.128
22
P SYN007 Synovitis 58 0.128
23
SCN006 Secondary Syphilis 53 0.128
24
c MYL007 Myeloma 53 0.128
25
EVN001 Evans' Syndrome 50 0.111
26
PRT092 Partial Androgen Insensitivity Syndrome 45 0.101
27
PRL042 Proliferating Trichilemmal Cyst 40 0.101
28
HNM001 Hinman's Syndrome 28 0.101
29
P PRS040 Prostate Cancer 76 0.091
30
P MLT019 Multiple Myeloma 76 0.091
31
P OST002 Osteoporosis 73 0.091
32
PRG004 Progeria 68 0.091
33
PLY012 Polyhydramnios 49 0.091
34
KRT012 Keratoderma 44 0.091
35
ANG037 Angiomatosis 37 0.091
36
P KRT056 Keratosis Palmoplantaris Striata I, Ad 25 0.091
37
HYP004 Hypercalcemia 69 0.079
38
P ART023 Arthropathy 65 0.079
39
P SYS005 Systemic Scleroderma 63 0.079
40
HMN010 Hemangioma 62 0.079
41
P MND007 Mandibuloacral Dysplasia 53 0.079
42
THR013 Thoracic Outlet Syndrome 53 0.079
43
c SCL016 Scleroderma 53 0.079
44
KLD001 Keloids 52 0.079
45
P EXP004 Exophthalmos 51 0.079
46
ANK001 Ankylosis 51 0.079
47
CMP053 Camptodactyly of Fingers 13 0.079
48
PRG025 Progeroid Syndrome, Penttinen Type 3 0.079
49
P RHM011 Rheumatoid Arthritis 83 0.064
50
BRN024 Bronchitis 71 0.064
51
ACN002 Acanthosis Nigricans 70 0.064
52
P OST018 Osteosarcoma 70 0.064
53
P SYS004 Systemic Mastocytosis 65 0.064
54
VSC011 Vasculitis 65 0.064
55
DSM004 Desmoid Tumor 63 0.064
56
PSY004 Psychotic Disorder 62 0.064
57
OLL001 Ollier Disease 62 0.064
58
P PRD008 Periodontitis 58 0.064
59
MYC002 Mycobacterium Avium Complex Disease 56 0.064
60
c EPN002 Ependymoma 54 0.064
61
SRC014 Sarcoma 54 0.064
62
LYM019 Lymphosarcoma 53 0.064
63
PYC001 Pycnodysostosis 52 0.064
64
c MNT147 Mental Retardation 51 0.064
65
KRT009 Keratosis 49 0.064
66
LYM022 Lymphangioma 49 0.064
67
c ACR001 Aicardi-Goutieres Syndrome 46 0.064
68
c HYP087 Hypotrichosis 41 0.064
69
SCH016 Schimke Immunoosseous Dysplasia 40 0.064
70
MYX001 Myxopapillary Ependymoma 39 0.064
71
PLM029 Palmoplantar Keratosis 38 0.064
72
TTR016 Tetra-Amelia Syndrome 36 0.064
73
LYM095 Lymphangiomatosis 30 0.064
74
c MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 26 0.064
75
NNS006 Non-Suppurative Otitis Media 24 0.064
76
HDG007 Hodgkin's Lymphoma 80 0.045
77
P HYP075 Hypertension 76 0.045
78
P PRM021 Primary Pulmonary Hypertension 74 0.045
79
P GCH001 Gaucher's Disease 73 0.045
80
LKM002 Leukemia 70 0.045
81
c MST009 Mastocytosis 67 0.045
82
c THR014 Thrombocytopenia 66 0.045
83
P LPR002 Leopard Syndrome 66 0.045
84
P SHR002 Short Stature 64 0.045
85
c LCL006 Localized Scleroderma 64 0.045
86
WST001 West Syndrome 64 0.045
87
c PRM002 Primary Hyperoxaluria 63 0.045
88
LNG024 Langerhans-Cell Histiocytosis 63 0.045
89
c JVN010 Juvenile Rheumatoid Arthritis 62 0.045
90
PLY017 Polyarteritis Nodosa 62 0.045
91
P HST010 Histiocytosis 61 0.045
92
MXD005 Mixed Connective Tissue Disease 60 0.045
93
DBT010 Diabetic Neuropathy 59 0.045
94
P OST001 Osteopetrosis 59 0.045
95
SQM006 Squamous Cell Carcinoma 58 0.045
96
ERD001 Erdheim-Chester Disease 58 0.045
97
P AGM001 Agammaglobulinemia 58 0.045
98
OCC006 Occipital Horn Syndrome 57 0.045
99
KDS001 Kid Syndrome 55 0.045
100
c EHL001 Ehlers-Danlos Syndrome 55 0.045
101
FLT001 Felty's Syndrome 54 0.045
102
LYM040 Lymphoblastic Lymphoma 54 0.045
103
NRP001 Neuropathy 54 0.045
104
P SNS014 Sinusitis 54 0.045
105
LPD010 Lipodystrophy 53 0.045
106
P SPN052 Spondyloarthropathy 52 0.045
107
P GNT008 Giant Cell Tumor 52 0.045
108
CRY005 Cryptococcosis 51 0.045
109
P PRT039 Proteinuria 51 0.045
110
P SPH001 Sapho Syndrome 51 0.045
111
FBR009 Fibrous Dysplasia 51 0.045
112
CNN005 Connective Tissue Disease 51 0.045
113
GNG012 Gingival Overgrowth 50 0.045
114
CLC006 Calcinosis 49 0.045
115
EXS001 Exostosis 49 0.045
116
MDS022 Mediastinitis 49 0.045
117
ANH002 Anhidrosis 48 0.045
118
PHC013 Phaeochromocytoma 48 0.045
119
FBR019 Fibromatosis 47 0.045
120
DFF003 Diffuse Scleroderma 47 0.045
121
DYS018 Dysostosis 45 0.045
122
c TYP003 Type I Ehlers-Danlos Syndrome 45 0.045
123
P VHW001 Vohwinkel Syndrome 45 0.045
124
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 44 0.045
125
FSC004 Fasciitis 44 0.045
126
BLC003 Bloch-Sulzberger Syndrome 44 0.045
127
INT191 Intestinal Lymphangiectasia 43 0.045
128
RLY001 Riley-Day Syndrome 43 0.045
129
ERY017 Erythema Elevatum Diutinum 41 0.045
130
RTR008 Root Resorption 41 0.045
131
RHM014 Rheumatoid Vasculitis 41 0.045
132
PPL006 Papillon-Lefevre Disease 41 0.045
133
PTY003 Pityriasis Rubra Pilaris 41 0.045
134
PGT004 Paget Disease, Juvenile 41 0.045
135
ORL015 Oral Squamous Cell Carcinoma 40 0.045
136
MNN014 Mononeuritis 40 0.045
137
ACT055 Actinomycosis 40 0.045
138
c TYP002 Type Vi Ehlers-Danlos Syndrome 40 0.045
139
LYM008 Lymphangiosarcoma 40 0.045
140
TND005 Tendinitis 40 0.045
141
AGG002 Aggressive Systemic Mastocytosis 39 0.045
142
c MLR003 Melorheostosis 37 0.045
143
MSS002 Mass Syndrome 37 0.045
144
PRM018 Primary Hypertrophic Osteoarthropathy 36 0.045
145
GCH006 Gaucher Disease Perinatal Lethal 35 0.045
146
c ATX010 Ataxia Neuropathy Spectrum 33 0.045
147
CRN077 Cranio Osteoarthropathy 33 0.045
148
P ATS061 Autosomal Recessive Hypotrichosis 32 0.045
149
ADS002 Adie Syndrome 32 0.045
150
MNN002 Mononeuritis Multiplex 31 0.045
151
ENC010 Encephalocraniocutaneous Lipomatosis 31 0.045
152
HMM002 Haim-Munk Syndrome 31 0.045
153
BNG036 Bone Giant Cell Tumor 31 0.045
154
P SLP004 Salpingo-Oophoritis 30 0.045
155
c GCH005 Gaucher Disease Type 3 30 0.045
156
P EHL009 Ehlers-Danlos Syndrome Type Iv 30 0.045
157
OLM001 Olmsted Syndrome 30 0.045
158
P GMM003 Gamma Heavy Chain Disease 30 0.045
159
P EXS004 Exostoses, Multiple, Type 1 29 0.045
160
P HRD033 Hereditary Sensory and Autonomic Neuropathy Type Ii 29 0.045
161
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 28 0.045
162
c FRN011 Frontal Sinusitis 28 0.045
163
HYL002 Hyalinosis, Inherited Systemic 27 0.045
164
GNT005 Giant Hemangioma 27 0.045
165
CRB079 Cerebrospinal Fluid Leak 27 0.045
166
EHL006 Ehlers–danlos Syndrome 27 0.045
167
c EHL041 Ehlers-Danlos Syndrome, Type Vii 26 0.045
168
c FRT001 Fourth Cranial Nerve Palsy 26 0.045
169
c LYM063 Lymphoma, Diffuse Large Cell 26 0.045
170
NNP003 Nonepidermolytic Palmoplantar Keratoderma 25 0.045
171
BNR002 Bone Resorption Disease 24 0.045
172
ZNC001 Zunich Neuroectodermal Syndrome 23 0.045
173
MLD003 Meleda Disease 23 0.045
174
P MYF007 Myofibromatosis, Infantile, 1 23 0.045
175
XNT009 Xanthoma Disseminatum 23 0.045
176
RCK007 Rickets, Vitamin D-Resistant, Type Iia 23 0.045
177
P ADL001 Adult Lymphoma 23 0.045
178
CLC004 Calcific Tendinitis 22 0.045
179
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 22 0.045
180
RMN002 Ramon Syndrome 20 0.045
181
AND005 Androgen Insensitivity Syndrome, Mild 19 0.045
182
PRD003 Periodontosis 18 0.045
183
MNS012 Monostotic Fibrous Dysplasia 18 0.045
184
c BNG076 Benign Exophthalmos Syndrome 17 0.045
185
c CHR040 Chronic Frontal Sinusitis 16 0.045
186
c ADL081 Adult Chronic Recurrent Multifocal Osteomyelitis 15 0.045
187
c JVN029 Juvenile Chronic Recurrent Multifocal Osteomyelitis 14 0.045
188
HSH001 Hashimoto-Pritzker Syndrome 13 0.045
189
DRM020 Dermatoosteolysis Kirghizian Type 13 0.045
190
c EHL028 Ehlers-Danlos Syndrome, Type Viii 11 0.045
191
INT170 Intellectual Deficit - Cataracts - Calcified Pinnae - Myopathy 11 0.045
192
CYT002 Cytokine Deficiency 11 0.045
193
ACR021 Aica-Ribosiduria Due to Atic Deficiency 10 0.045
194
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 9 0.045