Disease #01056 (JBTS10 (Joubert syndrome, type 10 (JBTS-10)), OMIM:300804)
Official abbreviation |
JBTS10 |
Name |
Joubert syndrome, type 10 (JBTS-10) |
OMIM ID |
300804 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
OFD1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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