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 |
1 |
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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|