developmental and epileptic encephalopathy 48

Summary
Synonym
  • DEE48
  • early infantile epileptic encephalopathy 48
Definition
A developmental and epileptic encephalopathy characterized by seizure onset before 1 year of age, global developmental delay, intellectual disability, absent speech, and minimal or absent motor development that has_material_basis_in homozygous or compound heterozygous mutation in the AP3B2 gene on chromosome 15q25.
Super Class
autosomal recessive disease developmental and epileptic encephalopathy
External Links
Disease Ontology
DOID:0080448
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8120 AP3B2 adaptor related protein complex 3 subunit beta 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
11775 Ap3b2 adaptor-related protein complex 3, beta 2 subunit
Displaying 1 entry
Gene ID Gene Symbol Description Source
853177 APL6 Apl6p
The Human Phenotype Ontology
Displaying entries 1 - 10 of 53 in total
HPO ID HPO Term
HP:0000054 Micropenis
HP:0000070 Ureterocele
HP:0000110 Renal dysplasia
HP:0000175 Cleft palate
HP:0000252 Microcephaly
HP:0000340 Sloping forehead
HP:0000463 Anteverted nares
HP:0000486 Strabismus
HP:0000729 Autistic behavior
HP:0000752 Hyperactivity
Displaying all 2 entries
Gene ID Gene Symbol Description
51227 PIGP phosphatidylinositol glycan anchor biosynthesis class P
9091 PIGQ phosphatidylinositol glycan anchor biosynthesis class Q

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024