Phenotypes for disease #04652 (MCPH14 (microcephaly?, type 14, primary, autosomal recessive (MCPH-14)), OMIM:616402)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000073509 Congenital microcephaly - - Familial, autosomal recessive - - - - - Karen Stals 00095114
0000268656 Microcephaly, Pachygyria, Lissencephaly - 1y Unknown - - - - - Andreas Laner 00373380
Legend   How to query  


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