Disease #04178 (LNMS (Laurence-Moon syndrome (LNMS)), OMIM:245800)

Official abbreviation LNMS
Name Laurence-Moon syndrome (LNMS)
OMIM ID 245800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PNPLA6
Associated tissues -
Disease features -
Remarks -
Date created 2015-01-27 14:11:39 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00029689 - PubMed: Hufnagel 2015, Journal: Hufnagel 2015 2-generation family, 1 affected, unaffected parents M - - - - - - - LNMS see paper; .. PNPLA6 PNPLA6 2 1 Johan den Dunnen
00029691 - PubMed: Chalvon-Demersay 1993, PubMed: Hufnagel 2015, Journal: Hufnagel 2015 2-generation family, 5 affecteds brothers/sisters (3F, 2M) - no France - - - - - LNMS see paper; ,, PNPLA6 PNPLA6 2 5 Johan den Dunnen
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