Search results for [ge] HDAC8

Showing 25 of 25 hits for [ge] HDAC8
# Family MCID Name MIFTS Score
1
c CRN209 Cornelia De Lange Syndrome 5 40 29.267
2
P CRN015 Cornelia De Lange Syndrome 66 26.296
3
c CRN139 Cornelia De Lange Syndrome 1 62 19.071
4
INT449 Intellectual Developmental Disorder, X-Linked, Syndromic, Wilson-Turner Type 49 15.601
5
P MCR010 Microcephaly 59 15.601
6
P FRN036 Frontonasal Dysplasia 1 55 10.218
7
P RTT002 Rett Syndrome 78 10.218
8
P ATR010 Atrial Heart Septal Defect 58 10.218
9
P FNC044 Fanconi Anemia, Complementation Group C 56 7.225
10
P SYN060 Syndactyly, Type Iii 44 7.225
11
RBR002 Roberts-Sc Phocomelia Syndrome 66 7.225
12
HYP748 Hypertelorism 50 7.225
13
KBG001 Kbg Syndrome 55 7.225
14
MTR088 Mature T-Cell and Nk-Cell Lymphoma 43 7.225
15
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 67 7.225
16
CRN320 Cornelia De Lange Syndrome 3 with or Without Midline Brain Defects 43 7.225
17
P CRN321 Cornelia De Lange Syndrome 4 with or Without Midline Brain Defects 45 7.225
18
WHT019 White-Sutton Syndrome 46 7.225
19
c CNG031 Congenital Nervous System Abnormality 32 7.225
20
FML286 Familial Isolated Trichomegaly 34 7.225
21
OPT062 Optic Atrophy 10 with or Without Ataxia, Mental Retardation, and Seizures 43 7.225
22
CHR515 Chronic Atrial and Intestinal Dysrhythmia 44 7.225
23
P PLY014 Polycystic Kidney Disease 70 7.225
24
EYL005 Eyelid Disease 41 7.225
25
INT276 Interatrial Communication 51 7.225
1
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