×
Entrez Id:
3190
Gene Symbol:
HNRNPK
HNRNPK
Intrauterine retardation
0.100
GeneticVariation
CLINVAR
×
Entrez Id:
64135
Gene Symbol:
IFIH1
IFIH1
Intrauterine retardation
0.100
CausalMutation
CLINVAR
An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1.
30965144
2020
×
Entrez Id:
3778
Gene Symbol:
KCNMA1
KCNMA1
Intrauterine retardation
0.100
CausalMutation
CLINVAR
KCNMA1-AS1
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
89953
Gene Symbol:
KLC4
KLC4
Intrauterine retardation
0.100
GeneticVariation
CLINVAR
Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome.
30980518
2019
×
Entrez Id:
4297
Gene Symbol:
KMT2A
KMT2A
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
54551
Gene Symbol:
MAGEL2
MAGEL2
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
25836
Gene Symbol:
NIPBL
NIPBL
Intrauterine retardation
0.100
GeneticVariation
CLINVAR
×
Entrez Id:
51633
Gene Symbol:
OTUD6B
OTUD6B
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
55023
Gene Symbol:
PHIP
PHIP
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
55163
Gene Symbol:
PNPO
PNPO
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
10585
Gene Symbol:
POMT1
POMT1
Intrauterine retardation
0.100
GeneticVariation
CLINVAR
×
Entrez Id:
54496
Gene Symbol:
PRMT7
PRMT7
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
54870
Gene Symbol:
QRICH1
QRICH1
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
100151683
Gene Symbol:
RNU4ATAC
RNU4ATAC
Intrauterine retardation
0.100
GeneticVariation
CLINVAR
×
Entrez Id:
100151683
Gene Symbol:
RNU4ATAC
RNU4ATAC
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
6329
Gene Symbol:
SCN4A
SCN4A
Intrauterine retardation
0.100
CausalMutation
CLINVAR
[The construction and preliminary investigation of the cell model of a novel mutation R675Q in the SCN4A gene identified in a Chinese family with normokalemic periodic paralysis].
19065518
2008
×
Entrez Id:
6329
Gene Symbol:
SCN4A
SCN4A
Intrauterine retardation
0.100
CausalMutation
CLINVAR
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.
15596759
2004
×
Entrez Id:
6659
Gene Symbol:
SOX4
SOX4
Intrauterine retardation
0.100
GeneticVariation
CLINVAR
De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.
30661772
2019
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Intrauterine retardation
0.100
CausalMutation
CLINVAR
×
Entrez Id:
7287
Gene Symbol:
TULP1
TULP1
Intrauterine retardation
0.100
CausalMutation
CLINVAR
Antioxidant effect of aqueous extract of four plants with therapeutic potential on gynecological diseases; Semen persicae, Leonurus cardiaca, Hedyotis diffusa, and Curcuma zedoaria.
29178942
2017