Disease #00579 (AO1 (atelosteogenesis, type I (AO-1)), OMIM:108720)
Official abbreviation |
AO1 |
Name |
atelosteogenesis, type I (AO-1) |
OMIM ID |
108720 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
31 |
Phenotype entries for this disease |
7 |
Associated with 1 gene |
FLNB |
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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|