Disease #00960 (NGPS (progeria syndrome, Nestor-Guillermo (NGPS)), OMIM:614008)

Official abbreviation NGPS
Name progeria syndrome, Nestor-Guillermo (NGPS)
OMIM ID 614008
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 BANF1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00151382 - PubMed: Puente 2011, PubMed: Cabanillas 2011 2-generation family, 1 affacted, third-cousin parents, unaffected heterozygous carrier parents M yes Spain - >31y - - - NGPS - BANF1 BANF1 5 1 Johan den Dunnen
00151383 - PubMed: Puente 2011, PubMed: Cabanillas 2011 2-generation family, 1 affacted, unaffected heterozygous carrier parents M no Spain - >24y - - - NGPS - BANF1 BANF1 1 1 Johan den Dunnen
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