Disease #06626 (MCPH18 (microcephaly 18, primary, autosomal dominant), OMIM:617520)
Official abbreviation |
MCPH18 |
Name |
microcephaly 18, primary, autosomal dominant |
OMIM ID |
617520 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
WDFY3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
2024-12-03 09:55:53 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|