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Search results for six3

184 hits were found for six3

# Family MCID Name MIFTS Score
1
c HLP024 Holoprosencephaly 2 49 48.353
2
P HLP001 Holoprosencephaly 68 42.685
3
SCH018 Schizencephaly 52 36.227
4
SLT005 Solitary Median Maxillary Central Incisor 50 21.729
5
SML028 Semilobar Holoprosencephaly 47 15.419
6
c HLP023 Holoprosencephaly 1 56 11.545
7
MCR013 Microphthalmia 59 11.294
8
P HYP083 Hypopituitarism 51 11.170
9
ANN002 Anencephaly 57 10.742
10
ALB014 Alobar Holoprosencephaly 45 8.617
11
CLB026 Colobomatous Microphthalmia 48 8.499
12
c HLP026 Holoprosencephaly 3 48 8.464
13
c HLP028 Holoprosencephaly 5 48 8.428
14
P ANR048 Aniridia 1 66 8.090
15
ATL016 Atelencephaly 13 8.018
16
P KLL001 Kallmann Syndrome 65 7.999
17
SPT006 Septooptic Dysplasia 62 7.945
18
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 44 7.869
19
LBR025 Lobar Holoprosencephaly 47 7.823
20
MCR173 Microform Holoprosencephaly 45 7.764
21
SPT016 Septopreoptic Holoprosencephaly 37 7.621
22
c HLP029 Holoprosencephaly 4 44 7.414
23
CLB010 Coloboma of Macula 53 7.238
24
PTS001 Patau Syndrome 55 7.205
25
HLP004 Holoprosencephaly, Recurrent Infections, and Monocytosis 28 7.062
26
CHR211 Chromosome 18p Deletion Syndrome 38 7.062
27
P PLL001 Pallister-Hall Syndrome 62 7.062
28
c HLP025 Holoprosencephaly 9 50 6.919
29
c ORF040 Orofaciodigital Syndrome Viii 49 6.919
30
P ORF002 Orofacial Cleft 43 6.919
31
P RTN008 Retinitis Pigmentosa 79 6.919
32
c HLP016 Holoprosencephaly 11 47 6.919
33
CLL036 Culler-Jones Syndrome 50 6.919
34
c HLP027 Holoprosencephaly 7 51 6.919
35
PHY002 Physical Disorder 40 6.919
36
c CNG031 Congenital Nervous System Abnormality 26 6.919
37
CRB034 Cerebral Hemisphere Lipoma 28 6.919
38
CNT024 Central Nervous System Lipoma 17 6.919
39
CRP003 Corpus Callosum Lipoma 35 6.919
40
IRS003 Iris Disease 31 6.919
41
P BRN006 Branchiootorenal Syndrome 51 6.919
42
FND002 Fundus Dystrophy 54 6.919
43
GLB002 Glioblastoma 67 1.626
44
HLX001 Helix Syndrome 47 1.578
45
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.509
46
P CHN012 Chondrosarcoma 56 1.490
47
CHN056 Chondrosarcoma, Extraskeletal Myxoid 42 1.490
48
P EXT030 Extraosseous Chondrosarcoma 31 1.490
49
P MYX008 Myxoid Chondrosarcoma 28 1.490
50
P INF032 Infertility 60 1.334
51
P LNG064 Lung Cancer Susceptibility 3 69 1.247
52
FRY006 Fryns Microphthalmia Syndrome 52 1.229
53
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 1.229
54
P ADN016 Adenocarcinoma 63 1.229
55
GLM045 Glioma 62 1.210
56
GLL048 Glial Tumor 51 1.210
57
P GLM040 Glioma Susceptibility 1 70 1.171
58
MLG169 Malignant Astrocytoma 57 1.171
59
ISL011 Isolated Aniridia 37 1.128
60
c SML038 Small Cell Cancer of the Lung 68 1.104
61
c MRG014 Meier-Gorlin Syndrome 6 25 1.104
62
P MRG008 Meier-Gorlin Syndrome 1 55 1.104
63
P LNG032 Lung Cancer 98 1.104
64
P MCR010 Microcephaly 59 1.104
65
CLF001 Cleft Lip 54 1.104
66
FML292 Familial Drusen 34 1.104
67
DWR001 Dwarfism 44 1.080
69
P RTN016 Retinal Degeneration 52 1.054
70
P MLN007 Male Infertility 56 1.026
71
P EYD002 Eye Disease 57 1.026
72
RRS010 Rare Soft Tissue Tumor 18 1.026
73
OPT070 Optic Nerve Hypoplasia, Bilateral 55 0.995
74
ISL109 Isolated Cleft Lip 33 0.923
75
c HYD064 Hydrocephalus, Congenital, 1 51 0.878
76
HRT030 Hartsfield Syndrome 46 0.878
77
c SPL067 Split-Hand/foot Malformation 1 46 0.878
78
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.878
79
LNG108 Langerhans Cell Histiocytosis 57 0.819
80
P HPT023 Hepatocellular Carcinoma 95 0.819
81
c RTN041 Retinitis Pigmentosa 11 43 0.819
82
HST010 Histiocytosis 49 0.819
83
P LNG021 Lung Occult Small Cell Carcinoma 20 0.768
84
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.768
85
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.768
86
P BRS047 Breast Cancer 97 0.734
87
CNG608 Congenital Hypopituitarism 29 0.676
88
P PNC035 Pancreatic Cancer 87 0.675
89
P OVR042 Ovarian Cancer 88 0.533
90
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.533
91
ESP021 Esophageal Cancer 84 0.494
92
NRL016 Neural Tube Defects 80 0.319
93
c MCR251 Microphthalmia, Syndromic 6 48 0.319
94
CHR178 Chromosomal Triplication 33 0.319
95
CLF004 Cleft Lip/palate 56 0.319
96
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.285
97
HYP080 Hypogonadism 49 0.285
98
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.247
99
P MYM013 Moyamoya Disease 1 59 0.247
100
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.247
101
HYP066 Hyperglycemia 60 0.247
102
OCL006 Ocular Hypertension 53 0.247
103
PTT001 Pituitary Hypoplasia 34 0.247
104
P DBT005 Diabetes Insipidus 54 0.247
105
PTT041 Pituitary Stalk Interruption Syndrome 54 0.247
106
CHN065 Choanal Atresia, Posterior 48 0.202
107
P PRS062 Persistent Hyperplastic Primary Vitreous 48 0.202
108
P RTN024 Retinoblastoma 72 0.202
109
PSD046 Pseudotrisomy 13 Syndrome 28 0.202
110
P PLY006 Polydactyly 58 0.202
111
PTR032 Peters-Plus Syndrome 63 0.202
112
c TBR025 Tuberous Sclerosis 1 84 0.202
113
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 0.202
114
CLF027 Cleft Palate, Isolated 64 0.202
115
P TBR001 Tuberous Sclerosis 69 0.202
116
P HYP730 Hypogonadotropic Hypogonadism 57 0.202
117
SBP001 Subependymal Giant Cell Astrocytoma 45 0.202
118
GNG004 Ganglioglioma 53 0.202
119
P RTN018 Retinal Disease 53 0.202
120
ALB002 Albinism 46 0.202
121
CNG562 Congenital Hypogonadotropic Hypogonadism 28 0.202
122
GRW007 Growth Hormone Deficiency 47 0.202
123
c ATS007 Autism Spectrum Disorder 71 0.143
124
c HGH032 High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 14 8 0.143
125
c DFN094 Deafness, Autosomal Dominant 28 31 0.143
126
P PTS002 Ptosis 52 0.143
127
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.143
128
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.143
129
c TYP009 Type 2 Diabetes Mellitus 91 0.143
130
OST159 Osteogenic Sarcoma 66 0.143
131
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.143
132
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.143
133
c DFN107 Deafness, Autosomal Dominant 10 40 0.143
134
MCR317 Macrophthalmia, Colobomatous, with Microcornea 18 0.143
135
P BRC006 Brachydactyly 52 0.143
136
P HGH038 High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6 12 0.143
137
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.143
138
P LSS002 Lissencephaly 52 0.143
139
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.143
140
P JBR020 Joubert Syndrome 1 74 0.143
141
SMT004 Smith-Lemli-Opitz Syndrome 69 0.143
142
c MCR115 Microvascular Complications of Diabetes 5 65 0.143
143
c HYP532 Hypogonadotropic Hypogonadism 18 with or Without Anosmia 27 0.143
144
c HYP522 Hypogonadotropic Hypogonadism 11 with or Without Anosmia 28 0.143
145
P HNT016 Huntington Disease 73 0.143
146
HYP748 Hypertelorism 46 0.143
147
HRW001 Hair Whorl 35 0.143
148
c HLP022 Holoprosencephaly 8 23 0.143
149
HMN047 Human Cytomegalovirus Infection 59 0.143
150
P VNT002 Ventricular Septal Defect 58 0.143
151
SQM006 Squamous Cell Carcinoma 59 0.143
152
HRT011 Heart Septal Defect 49 0.143
153
c HYP820 Hypogonadotropic Hypogonadism 22 with or Without Anosmia 24 0.143
154
ALT003 Alternating Exotropia 33 0.143
155
EXT022 Exotropia 42 0.143
156
P MYP006 Myopia 55 0.143
157
P LNS003 Lens Disease 35 0.143
158
P TRT010 Teratoma 50 0.143
159
GST033 Gestational Diabetes 60 0.143
160
P HYD006 Hydrocephalus 62 0.143
161
CRN027 Corneal Neovascularization 47 0.143
162
P CTR002 Cataract 59 0.143
163
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.143
164
EMP001 Empty Sella Syndrome 41 0.143
165
P RBL001 Rubella 58 0.143
166
c BRN138 Branchiootorenal Spectrum Disorder 20 0.143
167
47X002 47,xyy 47 0.143
168
48X005 48,xyyy 39 0.143
169
P ENC008 Encephalocele 46 0.143
170
c NNS019 Nonsyndromic Holoprosencephaly 16 0.143
171
PTT037 Pituitary Tumors 44 0.143
172
RTN123 Retinochoroidal Coloboma 19 0.143
174
P TRS029 Trisomy 1q 27 0.143
175
RFR003 Refractive Error 41 0.143
176
PNS014 Penis Agenesis 38 0.143
177
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 38 0.143
178
P VTR007 Vitreoretinopathy 45 0.143
179
CHR257 Chromosome 6q Deletion 15 0.143
180
CNG124 Congenital Rubella 43 0.143
181
EXN003 Exencephaly 30 0.143
182
HYD048 Hydrocephalus with Stenosis of the Aqueduct of Sylvius 37 0.143
183
P HYP265 Hypotonia 42 0.143
184
HYP266 Hypoxia 56 0.143
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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