Disease #01619 (ACG1A (achondrogenesis, type IA (ACG1A)), OMIM:200600)

Official abbreviation ACG1A
Name achondrogenesis, type IA (ACG1A)
OMIM ID 200600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TRIP11
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-01-13 11:07:57 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
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00132077 1 - - M no Brazil - - - - - ACG1A - TRIP11 TRIP11 2 1 Karina Silveira
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