Disease #05311 (LFIT2 (failure, liver, transient, infantile, type 2 (LFIT-2)), OMIM:616483)

Official abbreviation LFIT2
Name failure, liver, transient, infantile, type 2 (LFIT-2)
OMIM ID 616483
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene NBAS
Associated tissues -
Disease features -
Remarks -
Date created 2017-07-24 21:31:03 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00271297 ED2150 Ritelli et al., 2020 submitted - M no Italy - - - - - LFIT2, MRXSC, SOPH - CUL4B, NBAS CUL4B, NBAS 3 1 Marco Ritelli
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