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

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00415085 202299 - - M - Germany - - - - - MCPH18 neurodevelopmental delay, autistic behavior WDFY3 WDFY3 1 1 Andreas Laner
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.