Disease #00237 (ECTOL1 (ectopia lentis, type 1 (ECTOL-1)), OMIM:129600)
Official abbreviation |
ECTOL1 |
Name |
ectopia lentis, type 1 (ECTOL-1) |
OMIM ID |
129600 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
22 |
Phenotype entries for this disease |
16 |
Associated with 1 gene |
FBN1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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