Disease #04449 (DEE31A;EIEE31 (developmental and epileptic encephalopathy, type 31A), OMIM:616346)

Official abbreviation DEE31A;EIEE31
Name developmental and epileptic encephalopathy, type 31A
OMIM ID 616346
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease -
Associated with 1 gene DNM1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2024-11-11 21:51:31 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00435217 Pat1 PubMed: Liu 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents F no China Chinese - - - - DEE31A;EIEE31 - DNM1 DNM1 1 1 Min Peng
00435218 Pat2 PubMed: Liu 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents M no China Chinese - - - - DEE31A;EIEE31 - DNM1 DNM1 1 1 Min Peng
00435219 Pat3 PubMed: Liu 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents F no China Chinese - - - - DEE31A;EIEE31 - DNM1 DNM1 1 1 Min Peng
00435220 4 4 4 F - China Chinese - - - - DEE31A;EIEE31 - DNM1 DNM1 1 1 Min Peng
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