Disease #04015 (LDS5;RNHF (Loeys-Dietz syndrome, type 5 (LDS-5, Rienhoff syndrome (RNHF))), OMIM:615582)
| Official abbreviation |
LDS5;RNHF |
| Name |
Loeys-Dietz syndrome, type 5 (LDS-5, Rienhoff syndrome (RNHF)) |
| OMIM ID |
615582 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
TGFB3 |
| Associated tissues |
- |
| Disease features |
hypertelorism (HP:0000316); bifid uvula (HP:0000193)/cleft palate (HP:0000175); exotropia (HP:0000577); no craniosynostosis (-HP:0001363); cervical spine instability (HP:0010646); retrognathia (HP:0000278); scoliosis (HP:0002650); club foot (HP:0001762); osteoarthritis (HP:0002758); no pneumothorax (-HP:0002107); hernia (HP:0100790); no arterial tortuosity (-HP:0005116) |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-01-03 17:49:07 +01:00 (CET) |
Individuals
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