Search results for "otosclerosis, familial"

The MalaCard for "otosclerosis, familial" has been retired.
Searching MalaCards for entries containing "otosclerosis, familial"

101 hits were found for 'otosclerosis, familial'

# Family MCID Name MIFTS Score
1
P OTS001 Otosclerosis 35 0.948
2
SNS001 Sensorineural Hearing Loss 57 0.166
3
MSL001 Measles 61 0.155
4
P THY032 Thyroiditis 54 0.134
5
P OST002 Osteoporosis 64 0.107
6
CHL068 Cholestasis 59 0.105
7
ALR002 Al-Raqad Syndrome 36 0.103
8
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.101
9
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.098
10
ADT003 Auditory System Disease 40 0.098
11
P OST005 Osteogenesis Imperfecta 69 0.097
12
P EHL001 Ehlers-Danlos Syndrome 63 0.093
13
P ESP024 Esophagitis 61 0.088
14
ANK001 Ankylosis 51 0.086
15
OBS002 Obsessive-Compulsive Disorder 66 0.082
16
OTT002 Otitis Media 66 0.081
17
FBR012 Fabry Disease 69 0.080
18
URT039 Urticaria 57 0.078
19
HYP029 Hyperthyroxinemia 26 0.078
20
BSC001 Buschke-Ollendorff Syndrome 50 0.077
21
SPC005 Speech Disorder 41 0.077
22
DST005 Diastrophic Dysplasia 53 0.075
23
MDD010 Middle Ear Disease 48 0.075
24
P HYP086 Hypothyroidism 64 0.074
25
THY028 Thyroid Cancer 69 0.074
26
HPT074 Hepatic Adenoma, Somatic 50 0.074
27
INN002 Inner Ear Disease 49 0.073
28
NRM004 Neuroma 48 0.073
29
HNM002 Hinman Syndrome 25 0.070
30
CHR103 Charge Syndrome 62 0.067
31
P CMR001 Camurati-Engelmann Disease 58 0.067
32
EXS001 Exostosis 42 0.067
33
URT008 Urticaria Pigmentosa 37 0.067
34
P OST012 Osteoarthritis 83 0.066
35
GTR002 Goiter 52 0.066
36
P CHN012 Chondrosarcoma 56 0.065
37
CHL069 Cholesteatoma 49 0.063
38
CNT017 Central Nervous System Origin Vertigo 24 0.063
39
c CNG006 Congenital Hypothyroidism 60 0.062
40
MLK003 Melkersson-Rosenthal Syndrome 41 0.061
41
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.061
42
P HYP076 Hyperthyroidism 55 0.061
43
P SPS003 Spastic Diplegia 52 0.060
44
BNS002 Bone Structure Disease 37 0.060
45
ACS001 Acoustic Neuroma 58 0.060
46
ESP020 Esophageal Atresia 50 0.060
47
c OST135 Osteogenesis Imperfecta, Type I 46 0.060
48
END035 Endocrine Gland Cancer 49 0.060
49
P GRV001 Graves' Disease 59 0.058
50
P PND002 Pendred Syndrome 55 0.058
51
SPP008 Suppurative Otitis Media 45 0.058
52
PPL002 Papillary Carcinoma 51 0.055
53
ATM014 Autoimmune Disease of Endocrine System 36 0.055
54
P THY097 Thyroid Hormone Resistance 54 0.054
55
THY103 Thyroid Cancer, Monmedullary, 1 53 0.054
56
P ATX010 Ataxia Neuropathy Spectrum 30 0.054
57
ALL026 Allergic Hypersensitivity Disease 52 0.053
58
GNR008 Generalized Resistance to Thyroid Hormone 34 0.053
59
P TRN020 Turner Syndrome 65 0.052
60
MLT008 Multinodular Goiter 41 0.052
61
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.052
62
P URF003 Urofacial Syndrome 1 50 0.051
63
FBR009 Fibrous Dysplasia 45 0.051
64
P THY102 Thyroid Cancer, Nonmedullary, 2 58 0.049
65
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.048
66
THY030 Thyroid Gland Disease 48 0.048
67
c SBC007 Subacute Thyroiditis 40 0.048
68
c FML297 Familial Thyroid Dyshormonogenesis 31 0.048
69
MNR002 Meniere's Disease 48 0.047
70
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.047
71
c BRN108 Branchiootic Syndrome 1 34 0.047
72
HSH003 Hashimoto Thyroiditis 62 0.046
73
c OST121 Osteogenesis Imperfecta, Type Iv 48 0.046
74
PRN038 Prune Belly Syndrome 45 0.046
75
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 37 0.046
76
SPN033 Spontaneous Ocular Nystagmus 37 0.046
77
EXT056 External Ear Disease 36 0.046
78
END028 Endemic Goiter 35 0.046
79
BNG018 Benign Paroxysmal Positional Nystagmus 30 0.046
80
VST004 Vestibular Disease 44 0.044
81
c GRV008 Graves Disease 1 44 0.044
82
PLM011 Plummer's Disease 35 0.044
83
MYX004 Myxedema 35 0.044
84
NNT019 Neonatal Hypothyroidism 34 0.044
85
HRN022 Hearing Loss/deafness 26 0.044
86
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.042
87
CRB027 Cerebellar Disease 47 0.042
88
NDL007 Nodular Goiter 46 0.042
89
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 46 0.042
90
RGH009 Right Atrial Isomerism 44 0.042
91
THY049 Thyroid Cancer, Anaplastic 42 0.042
92
P MYS033 Miyoshi Muscular Dystrophy 1 42 0.042
93
OST004 Osteitis Fibrosa 41 0.042
94
ABR009 Abruzzo-Erickson Syndrome 38 0.042
95
c SPN103 Spinocerebellar Ataxia 31 38 0.042
96
P HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 36 0.042
97
NNT010 Nontoxic Goiter 35 0.042
98
ATH010 Athyreosis 31 0.042
99
PTH003 Pathologic Nystagmus 30 0.042
100
TXC004 Toxic Diffuse Goiter 28 0.042
101
SBC005 Subacute Lymphocytic Thyroiditis 17 0.042