Search results for msx1

106 hits were found for msx1

# Family MCID Name MIFTS Score
1
TTH002 Tooth Agenesis 60 4.976
2
WTK002 Witkop Syndrome 44 4.852
3
CLF001 Cleft Lip 53 4.507
4
c TTH010 Tooth Agenesis, Selective, 1 27 4.331
5
c ORF014 Orofacial Cleft 5 20 4.264
6
CLF027 Cleft Palate, Isolated 64 3.373
7
WLF002 Wolf-Hirschhorn Syndrome 59 2.897
8
P ORF002 Orofacial Cleft 44 2.814
9
CLF004 Cleft Lip/palate 54 2.713
10
CLF056 Cleft Lip with or Without Cleft Palate 47 2.612
11
P CRN037 Craniosynostosis 68 2.418
12
P ECT006 Ectodermal Dysplasia 62 2.366
13
ELL001 Ellis-Van Creveld Syndrome 62 2.335
14
P OMP004 Omphalocele 50 2.335
15
NRL016 Neural Tube Defects 82 2.298
16
P PRK057 Parkinson Disease, Late-Onset 78 2.298
17
CLF037 Cleft Lip/palate-Ectodermal Dysplasia Syndrome 51 2.298
18
CLF049 Cleft Lip and Alveolus 30 1.710
19
CHR619 Chromosome 2q35 Duplication Syndrome 62 1.673
20
P PRT042 Parietal Foramina 46 1.673
21
HYP791 Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate 43 1.673
22
ISL109 Isolated Cleft Lip 38 1.673
23
TTH032 Tooth Size 36 1.673
24
P TTR001 Tetralogy of Fallot 70 1.625
25
ODN023 Odontochondrodysplasia 68 1.625
26
CRZ001 Crouzon Syndrome 68 1.625
27
CHR103 Charge Syndrome 67 1.625
28
STH001 Saethre-Chotzen Syndrome 67 1.625
29
P TRC072 Treacher Collins Syndrome 1 66 1.625
30
DGR001 Digeorge Syndrome 64 1.625
31
P KLL001 Kallmann Syndrome 61 1.625
32
P VND007 Van Der Woude Syndrome 1 58 1.625
33
PPL025 Popliteal Pterygium Syndrome 56 1.625
34
HMF006 Hemifacial Microsomia 55 1.625
35
CLB010 Coloboma of Macula 52 1.625
36
LYM004 Lymphoid Interstitial Pneumonia 51 1.625
37
BRN003 Branchiooculofacial Syndrome 51 1.625
38
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 1.625
39
AND001 Anodontia 43 1.625
40
P SYN075 Syngnathia 43 1.625
41
PHY002 Physical Disorder 42 1.625
42
CLF053 Cleft Palate with or Without Ankyloglossia, X-Linked 37 1.625
43
CHR490 Chromosome 10q23 Deletion Syndrome 25 1.625
44
P PLY006 Polydactyly 59 0.116
45
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 31 0.100
46
P OVR042 Ovarian Cancer 88 0.082
47
P NRB001 Neuroblastoma 72 0.082
48
P LKM062 Leukemia, Acute Lymphoblastic 69 0.082
49
ADN018 Adenoma 59 0.082
50
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.082
51
BNR002 Bone Resorption Disease 48 0.082
52
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.082
53
TTH030 Teeth, Supernumerary 33 0.082
54
c TTH012 Tooth Agenesis, Selective, 3 26 0.082
55
CHR247 Chromosome 4p Deletion 22 0.082
57
P CLR023 Colorectal Cancer 99 0.058
58
c LKM061 Leukemia, Acute Myeloid 84 0.058
59
CRV035 Cervical Cancer 76 0.058
60
GLB015 Glioblastoma Multiforme 75 0.058
61
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.058
62
P FML011 Familial Adenomatous Polyposis 72 0.058
63
PRP027 Peripheral Vascular Disease 71 0.058
64
MNT001 Mantle Cell Lymphoma 69 0.058
65
RCK004 Rickets 68 0.058
66
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.058
67
P HYD006 Hydrocephalus 66 0.058
68
P NRV007 Nervous System Disease 66 0.058
69
BRR014 Barrett Esophagus 65 0.058
70
CLR108 Colorectal Adenoma 64 0.058
71
HYP066 Hyperglycemia 61 0.058
72
OST003 Osteonecrosis 61 0.058
73
c WLM018 Wilms Tumor 5 61 0.058
74
P BND020 Bone Disease 59 0.058
75
P INF032 Infertility 57 0.058
76
CHR003 Cherubism 57 0.058
77
HYP266 Hypoxia 57 0.058
78
DBL002 Double Outlet Right Ventricle 56 0.058
79
P PTT006 Pituitary Adenoma 55 0.058
80
P ART021 Arteriosclerosis 54 0.058
81
c CNT035 Central Nervous System Disease 52 0.058
82
P PRR016 Pierre Robin Syndrome 52 0.058
83
CLB002 Clubfoot 51 0.058
84
P HYP040 Hypospadias 51 0.058
85
ATS010 Autosomal Recessive Disease 48 0.058
86
HLX001 Helix Syndrome 47 0.058
87
c NLX003 Neu-Laxova Syndrome 2 47 0.058
88
RTN020 Retinal Vascular Disease 46 0.058
89
c SPL067 Split-Hand/foot Malformation 1 46 0.058
90
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.058
91
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.058
92
DWR001 Dwarfism 44 0.058
93
GNT001 Giant Cell Reparative Granuloma 41 0.058
94
OST115 Osteonecrosis of the Jaw 40 0.058
95
48X005 48,xyyy 39 0.058
96
OVR094 Ovarian Epithelial Cancer 38 0.058
97
c ECT072 Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type, Autosomal Dominant 37 0.058
98
HRW001 Hair Whorl 36 0.058
99
TRD003 Taurodontism 30 0.058
100
c HYP523 Hypogonadotropic Hypogonadism 14 with or Without Anosmia 30 0.058
101
ISL075 Isolated Pierre Robin Sequence 29 0.058
102
OLG005 Oligodontia-Colorectal Cancer Syndrome 28 0.058
103
P TTH013 Tooth Agenesis, Selective, 4 26 0.058
104
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 0.058
105
TTH029 Teeth Present at Birth 19 0.058
106
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.058
Content
Loading form....