Disease #00106 (AO2 (atelosteogenesis, type II (AO-2, De la Chapelle dysplasia)), OMIM:256050)

Official abbreviation AO2
Name atelosteogenesis, type II (AO-2, De la Chapelle dysplasia)
OMIM ID 256050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 4
Associated with 1 gene SLC26A2
Associated tissues -
Disease features -
Remarks -
Date created 2013-01-22 07:38:15 +01:00 (CET)
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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00006906 - - - - ? Netherlands - - - - - ACG1B, AO2, cancer, breast, cancer, predisposition, DYT, EDM4, EHT, MRLIAF, NBIA4, TMAU, TMD, WDM - BRCA1, BRCA2 BRCA1 1 1 Marjolijn JL Ligtenberg
00081682 - - - M no - - - - - - AO2 - SLC26A2 SLC26A2 2 1 Cynthia Silveira
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