IMP
Process View
Homo sapiens
10 genes annotated in human
pervasive developmental disorder
DOID:0060040
A developmental disorder of mental health that refers to a group of five disorders characterized by impairments in socialization and communication, as well as restricted interests and repetitive behaviors.
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In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "pervasive developmental disorder"
| Name | Description | Probability | Func Analog Organism | |
|---|---|---|---|---|
| EIF4EBP3 | eukaryotic translation initiation factor 4E binding protein 3 | 0.074 | ||
| CHD7 | chromodomain helicase DNA binding protein 7 | 0.031 | Human | |
| HIPK2 | homeodomain interacting protein kinase 2 | 0.024 | ||
| SMARCA2 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 | 0.021 | ||
| EIF4ENIF1 | eukaryotic translation initiation factor 4E nuclear import factor 1 | 0.015 | ||
| EIF4G1 | eukaryotic translation initiation factor 4 gamma, 1 | 0.013 | ||
| RBBP5 | retinoblastoma binding protein 5 | 0.012 | ||
| AMD1 | adenosylmethionine decarboxylase 1 | 0.011 | ||
| CASK | calcium/calmodulin-dependent serine protein kinase (MAGUK family) | 0.010 | ||
| CNTNAP2 | contactin associated protein-like 2 | 0.002 | ||
| NLGN4X | neuroligin 4, X-linked | 0.002 | ||
| FOXG1 | forkhead box G1 | 0.002 | ||
| TMLHE | trimethyllysine hydroxylase, epsilon | 0.002 | ||
| CHD8 | chromodomain helicase DNA binding protein 8 | 0.002 | ||
| MECP2 | methyl CpG binding protein 2 (Rett syndrome) | 0.001 | ||
| SHANK2 | SH3 and multiple ankyrin repeat domains 2 | 0.001 | ||
| NLGN3 | neuroligin 3 | 0.001 | ||
| RPL10 | ribosomal protein L10 | 0.001 | ||
| EIF4E | eukaryotic translation initiation factor 4E | 0.001 |