Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000188408 Individual ID 00249443 Associated disease SCKL Diagnosis/Initial - Diagnosis/Definite - Phenotype details primary microcephaly Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name REVY Database submission license No license selected Created by REVY Date created 2012-09-03 14:41:47 +02:00 (CEST) Date last edited 2012-09-08 20:32:13 +02:00 (CEST)

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