Search results for six3

76 hits were found for six3

# Family MCID Name MIFTS Score
1
c HLP024 Holoprosencephaly 2 49 5.509
2
SCH018 Schizencephaly 52 4.998
3
P HLP001 Holoprosencephaly 67 4.846
4
MCR013 Microphthalmia 57 2.442
5
ANN002 Anencephaly 56 2.442
6
P HYP083 Hypopituitarism 53 2.442
7
c HLP023 Holoprosencephaly 1 53 2.442
8
SLT005 Solitary Median Maxillary Central Incisor 49 2.442
9
SML028 Semilobar Holoprosencephaly 44 2.442
10
c HLP026 Holoprosencephaly 3 48 1.767
11
CLB026 Colobomatous Microphthalmia 47 1.767
12
c HLP028 Holoprosencephaly 5 45 1.767
13
ALB014 Alobar Holoprosencephaly 42 1.767
14
ATL016 Atelencephaly 13 1.767
15
SPT006 Septooptic Dysplasia 64 1.727
16
P ANR048 Aniridia 1 63 1.727
17
MCR173 Microform Holoprosencephaly 44 1.727
18
LBR025 Lobar Holoprosencephaly 43 1.727
19
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 40 1.727
20
SPT016 Septopreoptic Holoprosencephaly 33 1.727
21
P RTN008 Retinitis Pigmentosa 79 1.673
22
PLL001 Pallister-Hall Syndrome 64 1.673
23
PTS001 Patau Syndrome 55 1.673
24
CLB010 Coloboma of Macula 52 1.673
25
CLL036 Culler-Jones Syndrome 51 1.673
26
c ORF040 Orofaciodigital Syndrome Viii 50 1.673
27
c HLP025 Holoprosencephaly 9 50 1.673
28
c HLP016 Holoprosencephaly 11 47 1.673
29
c HLP029 Holoprosencephaly 4 44 1.673
30
P ORF002 Orofacial Cleft 44 1.673
31
PHY002 Physical Disorder 42 1.673
32
c HLP027 Holoprosencephaly 7 40 1.673
33
CRP003 Corpus Callosum Lipoma 34 1.673
34
IRS003 Iris Disease 29 1.673
35
ALT002 Aleutian Mink Disease 28 1.673
36
HLP004 Holoprosencephaly, Recurrent Infections, and Monocytosis 28 1.673
37
CRB034 Cerebral Hemisphere Lipoma 26 1.673
38
c CNG031 Congenital Nervous System Abnormality 24 1.673
39
CNT024 Central Nervous System Lipoma 21 1.673
40
GLB015 Glioblastoma Multiforme 75 0.091
41
P INF032 Infertility 57 0.091
42
P CHN012 Chondrosarcoma 56 0.091
43
HLX001 Helix Syndrome 47 0.091
44
CHN056 Chondrosarcoma, Extraskeletal Myxoid 46 0.091
45
P EXT030 Extraosseous Chondrosarcoma 35 0.091
46
P MYX008 Myxoid Chondrosarcoma 32 0.091
48
P LNG064 Lung Cancer Susceptibility 3 78 0.064
49
P LYN001 Lynch Syndrome 77 0.064
50
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.064
51
P ADN016 Adenocarcinoma 64 0.064
52
P GLM045 Glioma 63 0.064
53
P KLL001 Kallmann Syndrome 61 0.064
54
P MCR010 Microcephaly 59 0.064
55
EYD002 Eye Disease 58 0.064
56
LNG108 Langerhans Cell Histiocytosis 58 0.064
57
OPT070 Optic Nerve Hypoplasia, Bilateral 56 0.064
58
P MRG008 Meier-Gorlin Syndrome 1 55 0.064
59
P MLN007 Male Infertility 55 0.064
60
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.064
61
CLF001 Cleft Lip 53 0.064
62
FRY006 Fryns Microphthalmia Syndrome 52 0.064
63
P AST007 Astrocytoma 51 0.064
64
HST010 Histiocytosis 48 0.064
65
c SPL067 Split-Hand/foot Malformation 1 46 0.064
66
GLL048 Glial Tumor 45 0.064
67
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.064
68
HRT030 Hartsfield Syndrome 44 0.064
69
DWR001 Dwarfism 44 0.064
70
c RTN041 Retinitis Pigmentosa 11 42 0.064
71
ISL109 Isolated Cleft Lip 38 0.064
72
FML292 Familial Drusen 32 0.064
73
ISL011 Isolated Aniridia 31 0.064
74
c CNG608 Congenital Hypopituitarism 30 0.064
75
c MRG014 Meier-Gorlin Syndrome 6 25 0.064
76
RRS010 Rare Soft Tissue Tumor 18 0.064
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