Disease #03649 (ARCL3B (cutis laxa, autosomal recessive, type 3B (ARCL-3B)), OMIM:614438)

Official abbreviation ARCL3B
Name cutis laxa, autosomal recessive, type 3B (ARCL-3B)
OMIM ID 614438
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease -
Associated with 1 gene PYCR1
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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00222888 - - - - - - - - - - - ARCL3B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
00222889 - - - - - - - - - - - ARCL3B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
00222890 - - - - - - - - - - - ARCL3B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
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