Search results for cer1

39 hits were found for cer1

# Family MCID Name MIFTS Score
1
NRR002 Norrie Disease 61 13.648
2
CHR518 Chromosome 9p Deletion Syndrome 40 9.864
3
c KLF004 Kleefstra Syndrome 1 50 9.135
4
SVR004 Severe Combined Immunodeficiency 72 4.499
5
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 3.511
6
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 3.511
7
P OST002 Osteoporosis 76 2.638
8
P FBR017 Fibrosarcoma 56 2.420
9
CSY001 C Syndrome 61 2.310
10
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 2.310
11
SYN005 Synostosis 43 2.310
12
P CRN037 Craniosynostosis 68 2.310
13
FGF014 Fgfr Craniosynostosis Syndromes 25 2.310
14
CHL098 Childhood Myocerebrohepatopathy Spectrum 21 2.063
15
P TRT010 Teratoma 51 1.631
16
c KNN009 Kenny-Caffey Syndrome, Type 1 35 1.459
17
EMB004 Embryonal Carcinoma 56 1.459
18
P DRM053 Dermatitis, Atopic 65 1.032
19
IMM167 Immune Deficiency Disease 78 1.032
20
CMB007 Combined Immunodeficiency 57 1.032
21
P BRS047 Breast Cancer 98 0.753
22
P PNC035 Pancreatic Cancer 86 0.753
23
ART140 Arteries, Anomalies of 53 0.730
24
P CRN300 Coronary Heart Disease 1 73 0.730
25
LPP008 Lipoprotein Quantitative Trait Locus 65 0.730
26
NNL006 Non-Alcoholic Steatohepatitis 54 0.730
27
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.730
28
TRG015 Trigonocephaly 2 25 0.730
29
P RNG032 Ring Chromosome 39 0.730
30
CRN030 Coronary Stenosis 50 0.730
31
FTT001 Fatty Liver Disease 62 0.730
32
ISL084 Isolated Trigonocephaly 26 0.730
33
FRM011 Frem1 Autosomal Recessive Disorders 8 0.730
34
P HYP265 Hypotonia 42 0.730
35
c RNG025 Ring Chromosome 9 19 0.730
36
P OLG002 Oligodendroglioma 66 0.614
37
P ATS364 Autism 69 0.533
38
P LKM062 Leukemia, Acute Lymphoblastic 69 0.533
39
P EPL164 Epilepsy 68 0.533
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