Disease #06086 (JBTS32 (Joubert syndrome 32), OMIM:617757)
Official abbreviation |
JBTS32 |
Name |
Joubert syndrome 32 |
OMIM ID |
617757 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SUFU |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
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