Search results for six3

38 hits were found for six3

# Family MCID Name MIFTS Score
1
c HLP014 Holoprosencephaly-2 38 5.317
2
P HLP001 Holoprosencephaly 63 5.244
3
P SCH018 Schizencephaly 52 5.110
4
SNG010 Single Median Maxillary Central Incisor 52 3.510
5
SML028 Semilobar Holoprosencephaly 37 3.510
6
P MYM002 Moyamoya Disease 61 3.474
7
ANN002 Anencephaly 54 3.474
8
c SX3001 Six3-Related Holoprosencephaly 11 3.460
9
ALB014 Alobar Holoprosencephaly 35 3.049
10
LBR025 Lobar Holoprosencephaly 34 3.049
11
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 29 3.049
12
SPT016 Septopreoptic Holoprosencephaly 29 3.049
13
c FML149 Familial Schizencephaly, Six3-Related 5 3.049
14
PTS001 Patau Syndrome 49 3.008
15
P PRN026 Porencephaly 48 3.008
16
P HTR015 Heterotopia, Periventricular 46 3.008
17
SPS007 Spastic Cerebral Palsy 44 3.008
18
PHY002 Physical Disorder 43 3.008
19
CHR211 Chromosome 18p Deletion Syndrome 38 3.008
20
SPS005 Spastic Hemiplegia 38 3.008
21
c CNG031 Congenital Nervous System Abnormality 37 3.008
22
HYD001 Hydranencephaly 35 3.008
23
PSD001 Pseudobulbar Palsy 33 3.008
24
DYS001 Dyskinetic Cerebral Palsy 31 3.008
25
ENC005 Encephalomalacia 27 3.008
26
SPP007 Suppression Amblyopia 26 3.008
27
PRT006 Partial Motor Epilepsy 20 3.008
28
HLP004 Holoprosencephaly, Recurrent Infections, and Monocytosis 18 3.008
29
c FML302 Familial Schizencephaly, Shh-Related 20 2.614
30
SPT006 Septooptic Dysplasia 46 2.456
31
c DFN107 Deafness, Autosomal Dominant 10 41 2.456
32
c DFN094 Deafness, Autosomal Dominant 28 32 2.456
33
18P001 18p Deletion Syndrome 22 2.456
34
P CHN012 Chondrosarcoma 56 0.108
35
P MYX008 Myxoid Chondrosarcoma 31 0.108
36
P ADN016 Adenocarcinoma 69 0.076
37
P HST010 Histiocytosis 58 0.076
38
P HYP083 Hypopituitarism 54 0.076
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