Disease #00082 (JBTS9 (Joubert syndrome, type 9 (JBTS-9)), OMIM:612285)
Official abbreviation |
JBTS9 |
Name |
Joubert syndrome, type 9 (JBTS-9) |
OMIM ID |
612285 |
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 |
CC2D2A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-11-09 15:25:03 +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.
|