Disease #00997 (MGORS4 (Meier-Gorlin syndrome, type 4 (MGORS4)), OMIM:613804)
Official abbreviation |
MGORS4 |
Name |
Meier-Gorlin syndrome, type 4 (MGORS4) |
OMIM ID |
613804 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
CDT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-12-01 08:48:59 +01:00 (CET) |
Individuals
|