Disease #00203 (LDS4 (Loeys-Dietz syndrome, type 4 (LDS_4)), OMIM:614816)
Official abbreviation |
LDS4 |
Name |
Loeys-Dietz syndrome, type 4 (LDS_4) |
OMIM ID |
614816 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
TGFB2 |
Associated tissues |
- |
Disease features |
hypertelorism (HP:0000316); bifid uvula (HP:0000193)/cleft palate (HP:0000175); exotropia (HP:0000577); no craniosynostosis (-HP:0001363); no cervical spine instability (-HP:0010646); retrognathia (HP:0000278); scoliosis (HP:0002650); club foot (HP:0001762); osteoarthritis (HP:0002758); dural ectasia (HP:0100775); pneumothorax (HP:0002107); hernia (HP:0100790); dissection at young age; arterial tortuosity (HP:0005116) |
Remarks |
- |
Date created |
2013-09-20 17:42:46 +02:00 (CEST) |
Date last edited |
2022-01-03 17:48:35 +01:00 (CET) |
Individuals
|