Search results for six3

42 hits were found for six3

# Family MCID Name MIFTS Score
1
c HLP024 Holoprosencephaly 2 45 5.242
2
P HLP001 Holoprosencephaly 65 5.185
3
P SCH018 Schizencephaly 52 5.040
4
SML028 Semilobar Holoprosencephaly 36 3.008
5
P MYM002 Moyamoya Disease 60 2.968
6
ANN002 Anencephaly 53 2.968
7
c SX3001 Six3-Related Holoprosencephaly 11 2.911
8
CLB001 Coloboma 54 2.423
9
PTS001 Patau Syndrome 50 2.423
10
SPT006 Septooptic Dysplasia 48 2.423
11
P PRN026 Porencephaly 48 2.423
12
HTR015 Heterotopia, Periventricular 46 2.423
13
SNG010 Single Median Maxillary Central Incisor 45 2.423
14
SPS007 Spastic Cerebral Palsy 43 2.423
15
PHY002 Physical Disorder 43 2.423
16
c DFN107 Deafness, Autosomal Dominant 10 41 2.423
17
CHR211 Chromosome 18p Deletion Syndrome 40 2.423
18
c CNG031 Congenital Nervous System Abnormality 39 2.423
19
c HLP023 Holoprosencephaly 1 38 2.423
20
SPS005 Spastic Hemiplegia 37 2.423
21
HYD001 Hydranencephaly 35 2.423
22
c DFN094 Deafness, Autosomal Dominant 28 33 2.423
23
PSD001 Pseudobulbar Palsy 32 2.423
24
DYS001 Dyskinetic Cerebral Palsy 30 2.423
25
ENC005 Encephalomalacia 27 2.423
26
SPP007 Suppression Amblyopia 26 2.423
27
PRT006 Partial Motor Epilepsy 20 2.423
28
HLP004 Holoprosencephaly, Recurrent Infections, and Monocytosis 18 2.423
29
c FML302 Familial Schizencephaly, Shh-Related 20 1.930
30
ALB014 Alobar Holoprosencephaly 34 1.775
31
LBR025 Lobar Holoprosencephaly 34 1.775
32
MCR173 Microform Holoprosencephaly 31 1.775
33
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 29 1.775
34
SPT016 Septopreoptic Holoprosencephaly 29 1.775
35
c FML149 Familial Schizencephaly, Six3-Related 5 1.775
36
P CHN012 Chondrosarcoma 55 0.105
37
P MYX008 Myxoid Chondrosarcoma 29 0.105
38
P LYN001 Lynch Syndrome 71 0.074
39
P ADN016 Adenocarcinoma 69 0.074
40
P HST010 Histiocytosis 54 0.074
41
P HYP083 Hypopituitarism 54 0.074
42
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 53 0.074
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