Disease #05923 (HMLR (Heimler, syndrome (HMLR)))

Official abbreviation HMLR
Name Heimler, syndrome (HMLR)
OMIM ID -
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2021-04-26 11:49:08 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00361831 Pat46 PubMed: Bahena 2021 - F yes Iran - - - - - HMLR - - PEX26 1 2 Barbara Vona
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