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

178 hits were found for 'osteolysis'

# Family MCID Name MIFTS Score
1
GRH001 Gorham's Disease 33 5.557
2
TRG005 Torg Winchester Syndrome 46 5.406
3
PLY045 Polyostotic Osteolytic Dysplasia, Hereditary Expansile 23 4.698
4
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 23 4.327
5
HYP499 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 12 4.272
6
PTT018 Petit-Fryns Syndrome 13 3.843
7
TLP005 Talo-Patello-Scaphoid Osteolysis 12 3.428
8
MLT033 Multicentric Osteolysis Nephropathy 6 3.356
9
ACR082 Acro-Osteolysis-Keloid-Like Lesions-Premature Aging Syndrome 13 3.309
10
OST045 Osteolysis Syndrome Recessive 3 3.309
11
WNC001 Winchester Syndrome 37 2.893
12
CRP008 Carpo Tarsal Osteolysis Recessive 1 2.732
13
TLP002 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 1 2.732
14
MLT064 Multicentric Osteolysis of Torg 6 2.702
15
PHL009 Phalangeal Microgeodic Syndrome 7 1.949
16
PNT007 Penttinen-Aula Syndrome 6 1.949
17
NST002 Nestor-Guillermo Progeria Syndrome 20 1.910
18
VNB002 Van Bogaert-Hozay Syndrome 3 1.910
19
HJD001 Hajdu-Cheney Syndrome 57 0.162
20
P BRS047 Breast Cancer 105 0.140
21
P ART022 Arthritis 75 0.132
22
c MYL007 Myeloma 59 0.132
23
SCN006 Secondary Syphilis 55 0.132
24
P SYN007 Synovitis 59 0.114
25
PRT092 Partial Androgen Insensitivity Syndrome 53 0.105
26
PRL042 Proliferating Trichilemmal Cyst 38 0.105
27
P PRS040 Prostate Cancer 91 0.093
28
P MLT019 Multiple Myeloma 89 0.093
29
P OST002 Osteoporosis 77 0.093
30
PRG004 Progeria 77 0.093
31
PRS047 Prostatitis 62 0.093
32
PLY012 Polyhydramnios 49 0.093
33
P KRT056 Keratosis Palmoplantaris Striata I, Ad 33 0.093
34
HNM002 Hinman Syndrome 24 0.093
35
P SYS005 Systemic Scleroderma 69 0.081
36
HYP004 Hypercalcemia 69 0.081
37
P ART023 Arthropathy 66 0.081
38
c SCL016 Scleroderma 59 0.081
39
EVN001 Evans' Syndrome 54 0.081
40
P CRV039 Cervicitis 52 0.081
41
P EXP004 Exophthalmos 51 0.081
42
ANK001 Ankylosis 50 0.081
43
KRT012 Keratoderma 31 0.081
44
CMP053 Camptodactyly of Fingers 16 0.081
45
PRG025 Progeroid Syndrome, Penttinen Type 3 0.081
46
P RHM011 Rheumatoid Arthritis 91 0.066
47
P OST018 Osteosarcoma 81 0.066
48
BRN024 Bronchitis 76 0.066
49
ACN002 Acanthosis Nigricans 73 0.066
50
OLL001 Ollier Disease 70 0.066
51
P SYS004 Systemic Mastocytosis 70 0.066
52
PSY004 Psychotic Disorder 69 0.066
53
P HMN010 Hemangioma 68 0.066
54
VSC011 Vasculitis 67 0.066
55
P PRD008 Periodontitis 66 0.066
56
SRC014 Sarcoma 63 0.066
57
PYC001 Pycnodysostosis 61 0.066
58
MYC002 Mycobacterium Avium Complex Disease 57 0.066
59
MND007 Mandibuloacral Dysplasia 55 0.066
60
LYM019 Lymphosarcoma 54 0.066
61
KRT009 Keratosis 53 0.066
62
SCH016 Schimke Immunoosseous Dysplasia 49 0.066
63
c ACR001 Aicardi-Goutieres Syndrome 49 0.066
64
MYX001 Myxopapillary Ependymoma 46 0.066
65
c HYP087 Hypotrichosis 43 0.066
66
TTR016 Tetra-Amelia Syndrome 43 0.066
67
KLD001 Keloids 42 0.066
68
PLM029 Palmoplantar Keratosis 39 0.066
69
P MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 0.066
70
MNT147 Mental Retardation 35 0.066
71
NNS006 Non-Suppurative Otitis Media 26 0.066
72
HDG007 Hodgkin's Lymphoma 91 0.047
73
P HYP075 Hypertension 86 0.047
74
P PRM021 Primary Pulmonary Hypertension 82 0.047
75
P LKM002 Leukemia 79 0.047
76
P GCH001 Gaucher's Disease 79 0.047
77
LNG024 Langerhans-Cell Histiocytosis 75 0.047
78
c LPR002 Leopard Syndrome 72 0.047
79
P HST010 Histiocytosis 71 0.047
80
c PRM002 Primary Hyperoxaluria 68 0.047
81
c LCL006 Localized Scleroderma 68 0.047
82
PLY017 Polyarteritis Nodosa 68 0.047
83
DBT010 Diabetic Neuropathy 68 0.047
84
c THR014 Thrombocytopenia 67 0.047
85
GNG013 Gingivitis 67 0.047
86
c JVN010 Juvenile Rheumatoid Arthritis 67 0.047
87
MXD005 Mixed Connective Tissue Disease 65 0.047
88
WST001 West Syndrome 64 0.047
89
ERD001 Erdheim-Chester Disease 64 0.047
90
P DFF005 Diffuse Large B-Cell Lymphoma 63 0.047
91
FLT001 Felty's Syndrome 62 0.047
92
P AGM001 Agammaglobulinemia 61 0.047
93
NRP001 Neuropathy 61 0.047
94
SQM006 Squamous Cell Carcinoma 61 0.047
95
c EHL001 Ehlers-Danlos Syndrome 61 0.047
96
P GNT008 Giant Cell Tumor 60 0.047
97
P OST001 Osteopetrosis 60 0.047
98
LPD010 Lipodystrophy 59 0.047
99
DSM004 Desmoid Tumor 58 0.047
100
RLY001 Riley-Day Syndrome 58 0.047
101
CRY005 Cryptococcosis 57 0.047
102
CNN005 Connective Tissue Disease 57 0.047
103
GNG012 Gingival Overgrowth 57 0.047
104
OCC006 Occipital Horn Syndrome 57 0.047
105
P SHR002 Short Stature 57 0.047
106
PRT039 Proteinuria 57 0.047
107
P SPH001 Sapho Syndrome 56 0.047
108
MDS022 Mediastinitis 56 0.047
109
CLC006 Calcinosis 55 0.047
110
EXS001 Exostosis 54 0.047
111
PPL006 Papillon-Lefevre Disease 54 0.047
112
FBR009 Fibrous Dysplasia 54 0.047
113
DFF003 Diffuse Scleroderma 54 0.047
114
c ADL017 Adult T-Cell Leukemia 53 0.047
115
P SPN052 Spondyloarthropathy 52 0.047
116
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 52 0.047
117
KDS001 Kid Syndrome 52 0.047
118
BLC003 Bloch-Sulzberger Syndrome 52 0.047
119
ANH002 Anhidrosis 52 0.047
120
P EHL009 Ehlers-Danlos Syndrome Type Iv 51 0.047
121
FSC004 Fasciitis 50 0.047
122
DYS018 Dysostosis 49 0.047
123
PHC013 Phaeochromocytoma 49 0.047
124
c TCL004 T-Cell Leukemia 49 0.047
125
VHW001 Vohwinkel Syndrome 48 0.047
126
c TYP003 Type I Ehlers-Danlos Syndrome 48 0.047
127
MNN014 Mononeuritis 48 0.047
128
PTY003 Pityriasis Rubra Pilaris 47 0.047
129
AGG002 Aggressive Systemic Mastocytosis 47 0.047
130
c GCH005 Gaucher Disease Type 3 46 0.047
131
P ATX010 Ataxia Neuropathy Spectrum 44 0.047
132
LYM008 Lymphangiosarcoma 44 0.047
133
RTR008 Root Resorption 43 0.047
134
ACT055 Actinomycosis 42 0.047
135
TND005 Tendinitis 42 0.047
136
SYN053 Syndromic Diarrhea 42 0.047
137
GCH006 Gaucher Disease Perinatal Lethal 40 0.047
138
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 40 0.047
139
P EXS004 Exostoses, Multiple, Type 1 40 0.047
140
CRN077 Cranio Osteoarthropathy 39 0.047
141
P HRD033 Hereditary Sensory and Autonomic Neuropathy Type Ii 39 0.047
142
MLR003 Melorheostosis 38 0.047
143
PRM018 Primary Hypertrophic Osteoarthropathy 38 0.047
144
HYL002 Hyalinosis, Inherited Systemic 37 0.047
145
BNG036 Bone Giant Cell Tumor 35 0.047
146
P GMM003 Gamma Heavy Chain Disease 35 0.047
147
RCK007 Rickets, Vitamin D-Resistant, Type Iia 34 0.047
148
HMM002 Haim-Munk Syndrome 34 0.047
149
ADS002 Adie Syndrome 33 0.047
150
MNN002 Mononeuritis Multiplex 33 0.047
151
c FRN011 Frontal Sinusitis 32 0.047
152
ZNC001 Zunich Neuroectodermal Syndrome 32 0.047
153
P SLP004 Salpingo-Oophoritis 31 0.047
154
P MYF007 Myofibromatosis, Infantile, 1 31 0.047
155
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 31 0.047
156
NNP003 Nonepidermolytic Palmoplantar Keratoderma 31 0.047
157
OLM001 Olmsted Syndrome 31 0.047
158
c FRT001 Fourth Cranial Nerve Palsy 30 0.047
159
BNR002 Bone Resorption Disease 29 0.047
160
MLD003 Meleda Disease 29 0.047
161
GNT005 Giant Hemangioma 28 0.047
162
P ATS061 Autosomal Recessive Hypotrichosis 26 0.047
163
ENC010 Encephalocraniocutaneous Lipomatosis 25 0.047
164
P ADL001 Adult Lymphoma 24 0.047
165
CLC004 Calcific Tendinitis 23 0.047
166
RMN002 Ramon Syndrome 22 0.047
167
HSH001 Hashimoto-Pritzker Syndrome 22 0.047
168
c BNG076 Benign Exophthalmos Syndrome 21 0.047
169
PRD003 Periodontosis 20 0.047
170
c CHR040 Chronic Frontal Sinusitis 18 0.047
171
XNT009 Xanthoma Disseminatum 18 0.047
172
AND005 Androgen Insensitivity Syndrome, Mild 18 0.047
173
DRM020 Dermatoosteolysis Kirghizian Type 17 0.047
174
ACR021 Aica-Ribosiduria Due to Atic Deficiency 17 0.047
175
INT170 Intellectual Deficit - Cataracts - Calcified Pinnae - Myopathy 17 0.047
176
DRM037 Dermato-Cardio-Skeletal Syndrome, Borrone Type 16 0.047
177
c ADL081 Adult Chronic Recurrent Multifocal Osteomyelitis 15 0.047
178
c JVN029 Juvenile Chronic Recurrent Multifocal Osteomyelitis 15 0.047