Search results for "[genes] CDKN1C"

32 hits were found for '[genes] CDKN1C'

# Family MCID Name MIFTS Score
1
P BCK002 Beckwith-Wiedemann Syndrome 56 25.476
2
IMG001 Image Syndrome 50 22.063
3
P FCL005 Focal Segmental Glomerulosclerosis 60 18.014
4
HPT022 Hepatoblastoma 55 16.445
5
P SLV001 Silver-Russell Syndrome 54 16.445
6
CHR074 Choriocarcinoma 46 16.445
7
WLM007 Wilms Tumor Susceptibility-5 63 14.709
8
OMP004 Omphalocele 50 14.709
9
UMB002 Umbilical Hernia 44 14.709
10
c ADL052 Adult Acute Lymphocytic Leukemia 44 14.709
11
HYD046 Hydatidiform Mole, Recurrent, 1 41 14.709
12
P ANG001 Angelman Syndrome 61 12.738
13
c EXD008 Exudative Vitreoretinopathy 1 59 12.738
14
P GNG025 Gingival Fibromatosis 50 12.738
15
PYL017 Pyle Disease 45 12.738
16
MCR037 Macroglossia 45 12.738
17
GST052 Gestational Choriocarcinoma 42 12.738
18
HMH002 Hemihypertrophy 41 12.738
19
GRM001 Germ Cell and Embryonal Cancer 36 12.738
20
TRP005 Trophoblastic Neoplasm 36 12.738
21
c HRD009 Hereditary Wilms' Tumor 36 12.738
22
SLV005 Silver Spastic Paraplegia Syndrome 32 12.738
23
c SLV020 Silver-Russell Syndrome Due to a Point Mutation 13 12.738
24
FLL011 Fallopian Tube Gestational Choriocarcinoma 11 12.738
25
c BCK009 Beckwith-Wiedemann Syndrome Due to Cdkn1c Mutation 8 12.738
26
INT279 Intrauterine Growth Restriction-Short Stature-Early Adult-Onset Diabetes Syndrome 7 12.738
27
P ANT026 Anterior Segment Mesenchymal Dysgenesis 42 10.401
28
GST010 Gestational Trophoblastic Neoplasm 41 10.401
29
DNC004 Diencephalic Syndrome 33 10.401
30
c SPS027 Spastic Paraplegia 17 23 10.401
31
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 9 10.401
32
P EXD001 Exudative Vitreoretinopathy 47 7.354