Search results for neurog1

76 hits were found for neurog1

# Family MCID Name MIFTS Score
1
P SNS001 Sensorineural Hearing Loss 59 14.643
2
P ATS364 Autism 69 11.772
3
CCM004 Cecum Carcinoma 34 11.772
4
MBS002 Moebius Syndrome 54 10.592
5
HLX001 Helix Syndrome 48 9.607
6
ERM002 Ear Malformation 36 9.452
7
c DFN160 Deafness, Autosomal Dominant 52 25 8.975
8
CRB022 Cerebellar Liponeurocytoma 28 8.975
9
DSS008 Disease of Mental Health 74 8.324
10
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.753
11
c BRN108 Branchiootic Syndrome 1 62 3.584
12
P CLR023 Colorectal Cancer 100 3.417
13
ADN018 Adenoma 59 2.972
14
P MDL005 Medulloblastoma 75 2.765
15
SCH012 Schizoaffective Disorder 50 2.535
16
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.268
17
P TRT019 Torticollis 47 2.268
18
PLG004 Plagiocephaly 40 2.268
19
KRT006 Keratoconjunctivitis 53 2.114
20
P HYP265 Hypotonia 42 2.114
21
CHL065 Cholangiocarcinoma 58 1.724
22
INT079 Intrahepatic Cholangiocarcinoma 51 1.724
23
NRL016 Neural Tube Defects 81 1.457
24
EMB004 Embryonal Carcinoma 56 1.303
25
P MLN069 Melanoma, Uveal 61 1.128
26
P RTN024 Retinoblastoma 73 1.128
27
SKN019 Skin Melanoma 71 1.128
28
P MLN008 Melanoma 76 1.128
29
P OBS001 Obstructive Jaundice 48 1.128
30
PPL052 Papillomatosis, Confluent and Reticulated 34 0.921
31
CLT003 Colitis 63 0.921
32
CLR108 Colorectal Adenoma 64 0.921
33
ESP021 Esophageal Cancer 83 0.921
34
SPR008 Supratentorial Primitive Neuroectodermal Tumor 42 0.921
35
ULC004 Ulcerative Colitis 74 0.921
36
PNC129 Pancreatic Adenocarcinoma 65 0.921
37
P LYN001 Lynch Syndrome 76 0.921
38
P BRS047 Breast Cancer 98 0.851
39
P ALZ034 Alzheimer Disease 87 0.651
40
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.651
41
SPP011 Suppression of Tumorigenicity 12 61 0.651
42
MYC006 Mycosis Fungoides 65 0.651
43
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 51 0.651
44
P MLT020 Multiple Sclerosis 79 0.651
45
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.651
46
ATS010 Autosomal Recessive Disease 42 0.651
47
P CTN015 Cutaneous T Cell Lymphoma 48 0.651
48
c CNG012 Congenital Generalized Lipodystrophy 65 0.651
49
WRN001 Werner Syndrome 69 0.651
50
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.651
51
KPS004 Kaposi Sarcoma 77 0.651
52
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.651
53
c PCH010 Pachyonychia Congenita 3 43 0.651
54
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.651
55
P PRS040 Prostate Cancer 95 0.651
56
P GLM040 Glioma Susceptibility 1 71 0.651
57
CLR109 Colorectal Adenocarcinoma 50 0.651
58
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.651
59
PRM329 Premature Aging 36 0.651
60
THY029 Thyroid Carcinoma 51 0.651
61
P PTT014 Pitt-Hopkins Syndrome 64 0.651
62
GST040 Gastric Adenocarcinoma 67 0.651
63
P PLC011 Pilocytic Astrocytoma 57 0.651
64
P LNG064 Lung Cancer Susceptibility 3 70 0.651
65
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.651
66
THY122 Thyroid Gland Cancer 59 0.651
67
CLN015 Colon Adenocarcinoma 65 0.651
68
P ADN016 Adenocarcinoma 63 0.651
69
MLG169 Malignant Astrocytoma 57 0.651
70
P HYD006 Hydrocephalus 61 0.651
71
P MCR010 Microcephaly 60 0.651
72
P RCT021 Rectum Cancer 54 0.651
74
c BRN138 Branchiootorenal Spectrum Disorder 19 0.651
75
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.651
76
P PNC035 Pancreatic Cancer 86 0.602
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