Search results for cer1

40 hits were found for cer1

# Family MCID Name MIFTS Score
1
NRR002 Norrie Disease 59 13.113
2
CHR518 Chromosome 9p Deletion Syndrome 39 9.326
3
c KLF004 Kleefstra Syndrome 1 53 9.144
4
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.780
5
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.780
6
SVR004 Severe Combined Immunodeficiency 70 1.761
7
P OST002 Osteoporosis 76 1.297
8
CSY001 C Syndrome 61 1.215
9
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.215
10
P CRN037 Craniosynostosis 67 1.215
11
SYN005 Synostosis 43 1.215
12
FGF014 Fgfr Craniosynostosis Syndromes 26 1.215
13
P BRS047 Breast Cancer 97 0.753
14
P PNC035 Pancreatic Cancer 87 0.753
15
P OLG002 Oligodendroglioma 66 0.613
16
P FBR017 Fibrosarcoma 55 0.603
17
P ATS364 Autism 72 0.533
18
P LKM062 Leukemia, Acute Lymphoblastic 69 0.533
19
P EPL164 Epilepsy 70 0.533
20
CHL098 Childhood Myocerebrohepatopathy Spectrum 21 0.514
21
P TRT010 Teratoma 50 0.406
22
c KNN009 Kenny-Caffey Syndrome, Type 1 35 0.364
23
EMB004 Embryonal Carcinoma 55 0.364
24
P DRM053 Dermatitis, Atopic 65 0.257
25
IMM167 Immune Deficiency Disease 76 0.257
26
CMB007 Combined Immunodeficiency 56 0.257
27
P CRN300 Coronary Heart Disease 1 73 0.182
28
ART140 Arteries, Anomalies of 52 0.182
29
LPP008 Lipoprotein Quantitative Trait Locus 65 0.182
30
TRG015 Trigonocephaly 2 25 0.182
31
NNL006 Non-Alcoholic Steatohepatitis 54 0.182
32
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.182
33
CRN030 Coronary Stenosis 50 0.182
34
FTT001 Fatty Liver Disease 61 0.182
35
FRM011 Frem1 Autosomal Recessive Disorders 8 0.182
36
SFT003 Soft Tissue Sarcoma 43 0.182
37
c RNG025 Ring Chromosome 9 19 0.182
38
P HYP265 Hypotonia 42 0.182
39
ISL084 Isolated Trigonocephaly 26 0.182
40
P RNG032 Ring Chromosome 39 0.182
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