Disease #04190 (CODAS (cerebral, ocular, dental, auricular, skeletal syndrome (CODAS)), OMIM:600373)
Official abbreviation |
CODAS |
Name |
cerebral, ocular, dental, auricular, skeletal syndrome (CODAS) |
OMIM ID |
600373 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
10 |
Phenotype entries for this disease |
10 |
Associated with 1 gene |
LONP1 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2015-02-14 17:17:23 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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