Disease #04177 (OMCS (Oliver-McFarlane syndrome (OMCS)), OMIM:275400)

Official abbreviation OMCS
Name Oliver-McFarlane syndrome (OMCS)
OMIM ID 275400
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene PNPLA6
Associated tissues -
Disease features -
Remarks -
Date created 2015-01-27 14:10:39 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00029684 - PubMed: Hufnagel 2015, Journal: Hufnagel 2015 2-generation family, 2 affecteds (brother/sister), unaffected carrier parents - - - - - - - - OMCS Laurence-Moon syndrome considered; see paper; ... PNPLA6 PNPLA6 2 2 Johan den Dunnen
00029687 - PubMed: Hufnagel 2015, Journal: Hufnagel 2015 2-generation family, 1 affected, unaffected parents M - - - - - - - OMCS see paper; ... PNPLA6 PNPLA6 2 1 Johan den Dunnen
00029688 - PubMed: Hufnagel 2015, Journal: Hufnagel 2015 2-generation family, 1 affected, unaffected parents M - - - - - - - OMCS see paper; .. PNPLA6 PNPLA6 2 1 Johan den Dunnen
00029690 - PubMed: Patton 1986, PubMed: Hufnagel 2015, Journal: Hufnagel 2015 2-generation family, 1 affected, unaffected parents M - - white - - - - OMCS see paper .. PNPLA6 PNPLA6 2 1 Johan den Dunnen
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