Disease #05886 (PEBEL (encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy (PEBEL)))

Official abbreviation PEBEL
Name encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy (PEBEL)
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 2 genes APOA1BP, CARKD
Associated tissues -
Disease features -
Remarks -
Date created 2020-12-29 10:54:33 +01:00 (CET)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
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00314930 - - - F yes India - 03y - - - PEBEL - - CARKD 1 1 Anju Shukla
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