Search results for IRF6

66 hits were found for IRF6

# Family MCID Name MIFTS Score
1
PPL025 Popliteal Pterygium Syndrome 56 7.306
2
P VND007 Van Der Woude Syndrome 1 58 7.301
3
c ORF025 Orofacial Cleft 6 24 6.237
4
CLF001 Cleft Lip 53 4.878
5
CLF027 Cleft Palate, Isolated 64 4.378
6
TTH002 Tooth Agenesis 60 4.096
7
P ORF002 Orofacial Cleft 44 3.989
8
CLF004 Cleft Lip/palate 54 3.579
9
ISL109 Isolated Cleft Lip 38 2.620
10
CLF056 Cleft Lip with or Without Cleft Palate 47 2.438
11
P CNR004 Cone-Rod Dystrophy 2 73 2.432
12
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 2.432
13
P SYN075 Syngnathia 43 2.432
15
c ORF028 Orofacial Cleft 10 25 2.196
16
BRT059 Bartsocas-Papas Syndrome 46 1.852
17
CHR619 Chromosome 2q35 Duplication Syndrome 62 1.817
18
FCL090 Facial Cleft 34 1.775
19
CLF049 Cleft Lip and Alveolus 30 1.775
20
P KBK002 Kabuki Syndrome 1 67 1.719
21
P KLL001 Kallmann Syndrome 61 1.719
22
TRC003 Trichomoniasis 53 1.719
23
LYM004 Lymphoid Interstitial Pneumonia 51 1.719
24
BRN003 Branchiooculofacial Syndrome 51 1.719
25
BBS001 Babesiosis 48 1.719
26
HYP596 Hypophosphatasia, Childhood 48 1.719
27
FTL075 Fetal Encasement Syndrome 46 1.719
28
ANK017 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate 46 1.719
29
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 1.719
30
PHY002 Physical Disorder 42 1.719
31
c ORF016 Orofacial Cleft 8 39 1.719
32
CLF028 Cleft Soft Palate 37 1.719
33
ENM001 Enamel Caries 28 1.719
34
TTH005 Teeth Hard Tissue Disease 24 1.719
35
c ACT030 Acute Dacryoadenitis 18 1.719
36
VRL011 Viral Infectious Disease 61 0.094
37
HLX001 Helix Syndrome 47 0.094
38
P HYP265 Hypotonia 43 0.094
39
c VND004 Van Der Woude Syndrome 2 24 0.094
40
P GST053 Gastric Cancer 83 0.067
41
P MLT020 Multiple Sclerosis 72 0.067
42
OTT002 Otitis Media 72 0.067
43
P CRN037 Craniosynostosis 68 0.067
44
P NSP012 Nasopharyngeal Carcinoma 66 0.067
45
P HYD006 Hydrocephalus 66 0.067
46
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.067
47
P PRD008 Periodontitis 64 0.067
48
P ECT006 Ectodermal Dysplasia 62 0.067
49
P SNS001 Sensorineural Hearing Loss 60 0.067
50
c BNG091 Benign Chronic Pemphigus 58 0.067
51
DNT012 Dental Caries 53 0.067
52
P HYP040 Hypospadias 51 0.067
53
VLV034 Vulva Squamous Cell Carcinoma 48 0.067
54
c SPL067 Split-Hand/foot Malformation 1 46 0.067
55
P ECT100 Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 1 46 0.067
56
GRW007 Growth Hormone Deficiency 46 0.067
57
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.067
58
VLV044 Vulvar Intraepithelial Neoplasia 44 0.067
59
ORL015 Oral Squamous Cell Carcinoma 43 0.067
60
LCH016 Lichen Sclerosus Et Atrophicus 41 0.067
61
P SPL061 Split Hand-Foot Malformation 40 0.067
62
c CHR020 Chronic Interstitial Cystitis 37 0.067
63
HRW001 Hair Whorl 36 0.067
64
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.067
65
TTH030 Teeth, Supernumerary 33 0.067
66
CNT114 Central Nervous System Malformation 16 0.067
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