Disease #01416 (FPLD2 (lipodystrophy, familial partial, type 2 (FPLD-2)), OMIM:151660)

Official abbreviation FPLD2
Name lipodystrophy, familial partial, type 2 (FPLD-2)
OMIM ID 151660
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene LMNA
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

3 entries on 1 page. Showing entries 1 - 3.
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00165051 4 van Tienen, submitted - F ? Netherlands - >51y - - - FPLD2 - LMNA LMNA 1 1 Florence van Tienen
00165052 5 van Tienen, submitted - ? - - - - - - - FPLD2 - LMNA LMNA 1 1 Florence van Tienen
00234340 David Araujo-Vilar - - ? no Spain white - - - - FPLD2 - LMNA LMNA 1 1 David Araujo-Vilar
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