Disease #02426 (EE (ethylmalonic encephalopathy), OMIM:602473)

Official abbreviation EE
Name ethylmalonic encephalopathy
OMIM ID 602473
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ETHE1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00080947 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - EE Ethylmalonic encephalopathy (OMIM:602473) ETHE1 ETHE1 1 1 Daniel Trujillano
00466856 NDAR03-1 - 2 affected (2M), unaffected carrier parents M yes Pakistan South asian - - - - EE intellectual disability (HP:0010864), Muscular hypotonia (HP:0001252), facial dysmorphism (HP:0001999), and , delayed global milestones(HP:0001263), aggression - ETHE1 1 2 Arisha Rasheed
00466857 NDAR03-2 - sib M yes Pakistan Asia-S - - - - EE Intellectual disability (HP:0010864), Muscular hypotonia (HP:0001252), facial dysmorphism (HP:0001999), and , delayed global milestones(HP:0001263), seizures - ETHE1 1 1 Arisha Rasheed
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