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Joubert syndrome 6
Summary
- Synonym
-
- JBTS6
- Definition
- A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM67 gene on chromosome 8q22.
- Super Class
- Joubert syndrome
External Links
- Disease Ontology
- DOID:0111001
- Mondo Disease Ontology
- MeSH
- OMIM
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000426 | Prominent nasal bridge |
| HP:0001337 | Tremor |
| HP:0002553 | Highly arched eyebrow |
| HP:0001161 | Hand polydactyly |
| HP:0008872 | Feeding difficulties in infancy |
| HP:0007370 | Aplasia/Hypoplasia of the corpus callosum |
| HP:0030680 | Abnormal cardiovascular system morphology |
