Search results for fmn1

62 hits were found for fmn1

# Family MCID Name MIFTS Score
1
CHR619 Chromosome 2q35 Duplication Syndrome 64 13.838
2
SYN005 Synostosis 43 13.838
3
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 10.445
4
P WSK001 Wiskott-Aldrich Syndrome 72 10.445
5
RNL025 Renal Hypoplasia 41 10.445
6
ASP005 Asphyxiating Thoracic Dystrophy 47 10.445
7
P FCL005 Focal Segmental Glomerulosclerosis 57 10.445
8
P ACR072 Acrorenal Syndrome 33 7.386
9
P SYN060 Syndactyly, Type Iii 41 7.386
10
RCK002 Rocky Mountain Spotted Fever 34 7.386
11
c ATS005 Autosomal Dominant Nonsyndromic Deafness 24 7.386
12
c FCL025 Focal Segmental Glomerulosclerosis 1 49 7.386
13
c LTH026 Lethal Congenital Contracture Syndrome 4 33 7.386
14
MYS061 Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency 51 7.386
15
ADT007 Auditory Neuropathy, Autosomal Dominant, 1 34 7.386
16
P STR020 Strabismus 56 7.386
17
P RNL100 Renal Hypodysplasia/aplasia 1 63 7.386
18
CRY030 Cryptophthalmos, Unilateral or Bilateral, Isolated 38 7.386
19
DFN384 Deafness, Autosomal Dominant 1, with or Without Thrombocytopenia 44 7.386
20
P CNG001 Congenital Myasthenic Syndrome 68 7.386
21
FRS001 Far Eastern Spotted Fever 24 7.386
22
P CHR071 Charcot-Marie-Tooth Disease 64 7.386
23
P RDL002 Radioulnar Synostosis 47 2.633
24
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.633
25
P PNC035 Pancreatic Cancer 86 2.151
26
P CHN012 Chondrosarcoma 57 2.138
27
DWR001 Dwarfism 44 2.138
28
P FML011 Familial Adenomatous Polyposis 71 2.122
29
P RTN024 Retinoblastoma 73 1.886
30
CNN011 Cenani-Lenz Syndactyly Syndrome 51 0.980
31
P BRS047 Breast Cancer 98 0.779
32
OBS002 Obsessive-Compulsive Disorder 68 0.713
33
P OST002 Osteoporosis 76 0.713
34
c PNC108 Pancreatitis, Hereditary 69 0.713
35
ALC007 Alcohol Dependence 66 0.713
36
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.713
37
c MCR115 Microvascular Complications of Diabetes 5 65 0.713
38
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.713
39
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.713
40
P MCR129 Microvascular Complications of Diabetes 1 68 0.713
41
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.713
42
c SML038 Small Cell Cancer of the Lung 69 0.713
43
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.713
44
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.713
45
MNN043 Meningioma, Familial 79 0.713
46
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.713
47
P ALC033 Alcohol Use Disorder 61 0.713
48
P THR014 Thrombocytopenia 66 0.713
49
P OLG002 Oligodendroglioma 66 0.713
50
P BRS044 Breast Adenocarcinoma 58 0.713
51
ADN018 Adenoma 59 0.713
52
SCR001 Secretory Meningioma 40 0.713
53
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.713
54
c MCR112 Microvascular Complications of Diabetes 2 42 0.713
55
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.713
56
CNG034 Congestive Heart Failure 69 0.713
57
P PNC044 Pancreatitis 61 0.713
58
SPN021 Spinal Meningioma 50 0.713
59
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.713
60
SBS004 Substance Dependence 47 0.713
61
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.551
62
GLM045 Glioma 63 0.551
Content
Loading form....