Search results for TMEM38B

30 hits were found for TMEM38B

# Family MCID Name MIFTS Score
1
c OST109 Osteogenesis Imperfecta, Type Xiv 32 30.062
2
BRT054 Brittle Bone Disorder 74 26.238
3
P DNT011 Dentinogenesis Imperfecta 52 14.982
4
c OST121 Osteogenesis Imperfecta, Type Iv 49 8.714
5
P CLC057 Cole-Carpenter Syndrome 41 8.442
6
ODN023 Odontochondrodysplasia 67 8.442
7
P BRC015 Bruck Syndrome 48 8.442
8
P BND014 Bone Development Disease 33 8.442
9
P BND020 Bone Disease 59 3.597
10
c OST132 Osteogenesis Imperfecta, Type Vi 45 2.152
11
BNR002 Bone Resorption Disease 47 1.910
12
c OST119 Osteogenesis Imperfecta, Type Vii 49 1.910
13
P CXV002 Coxa Vara 33 1.910
14
EXP004 Exophthalmos 51 1.910
15
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.910
16
P HYP265 Hypotonia 42 1.910
17
P MLN069 Melanoma, Uveal 61 1.319
18
P MLN008 Melanoma 76 1.319
19
MLG142 Malignant Conjunctival Melanoma 37 1.319
20
OCL022 Ocular Melanoma 52 1.319
21
SKL017 Skeletal Dysplasias 41 1.077
22
FNC009 Fanconi-Bickel Syndrome 53 0.761
23
P MNR014 Menarche, Age at, Quantitative Trait Locus 2 7 0.761
24
c MNR015 Menarche, Age at, Quantitative Trait Locus 3 6 0.761
25
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.761
26
CLR030 Clear Cell Renal Cell Carcinoma 54 0.761
27
LYS002 Lysosomal Storage Disease 51 0.761
28
MCP033 Mucopolysaccharidoses 44 0.761
29
P BRS047 Breast Cancer 98 0.602
30
P PNC035 Pancreatic Cancer 86 0.602
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