Search results for "[genes] CDKN1C"

27 hits were found for '[genes] CDKN1C'

# Family MCID Name MIFTS Score
1
P BCK002 Beckwith-Wiedemann Syndrome 58 25.097
2
IMG001 Image Syndrome 56 22.701
3
P FCL005 Focal Segmental Glomerulosclerosis 65 15.134
4
P SLV001 Silver-Russell Syndrome 58 15.134
5
MTP001 Metaphyseal Dysplasia 46 15.134
6
OMP004 Omphalocele 46 15.134
7
MYL009 Myelodysplastic Syndrome 69 13.106
8
WLM007 Wilms Tumor Susceptibility-5 61 13.106
9
GST010 Gestational Trophoblastic Neoplasm 46 13.106
10
MCR037 Macroglossia 44 13.106
11
CHR074 Choriocarcinoma 43 13.106
12
c ADL052 Adult Acute Lymphocytic Leukemia 36 13.106
13
UMB002 Umbilical Hernia 35 13.106
14
P ANG001 Angelman Syndrome 66 10.701
15
c EXD008 Exudative Vitreoretinopathy 1 50 10.701
16
HMH002 Hemihypertrophy 45 10.701
17
TRP005 Trophoblastic Neoplasm 37 10.701
18
HYD046 Hydatidiform Mole, Recurrent, 1 33 10.701
19
c HRD009 Hereditary Wilms' Tumor 29 10.701
20
GRM001 Germ Cell and Embryonal Cancer 22 10.701
21
FLL011 Fallopian Tube Gestational Choriocarcinoma 9 10.701
22
c DFN258 Deafness, Autosomal Recessive 48 26 7.567
23
c USH031 Usher Syndrome, Type Ij 24 7.567
24
c WLM005 Wilms Tumor 2 15 7.567
25
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 10 7.567
26
c BCK009 Beckwith-Wiedemann Syndrome Due to Cdkn1c Mutation 9 7.567
27
c SLV020 Silver-Russell Syndrome Due to a Point Mutation 6 7.567