Disease #03214 (ARCL2B (cutis laxa, autosomal recessive, type 2B (ARCL-2B)), OMIM:612940)

Official abbreviation ARCL2B
Name cutis laxa, autosomal recessive, type 2B (ARCL-2B)
OMIM ID 612940
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
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

5 entries on 1 page. Showing entries 1 - 5.
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00222883 - - - - - - - - - - - ARCL2B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
00222884 - - - - - - - - - - - ARCL2B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
00222885 - - - - - - - - - - - ARCL2B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
00222886 - - - - - - - - - - - ARCL2B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
00222887 - - - - - - - - - - - ARCL2B - PYCR1 PYCR1 1 1 SIB - Livia Famiglietti
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