Disease #03948 (ILFS1 (liver failure syndrome, infantile, type 1), OMIM:615438)

Official abbreviation ILFS1
Name liver failure syndrome, infantile, type 1
OMIM ID 615438
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LARS
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

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00327416 172369 - - M ? Germany - - - - - ILFS1 (+) Acute encephalopathy,(+) Acute necrotizing encephalopathy; Fever, vomiting, rapid deterioration to coma, cMRI bithalamic space-occupying lesions compatible with encephalitis. LARS LARS 2 1 Andreas Laner
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