Global Variome shared LOVD

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

Phenotype #0000243069 Individual ID 00324525 Associated disease MGORS Phenotype details short stature microcephaly microtia congenital lobar emphysema myopia Diagnosis/Initial MGORS Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Louise Bicknell Database submission license No license selected Created by Louise Bicknell Date created 2020-12-18 04:14:53 +01:00 (CET) Date last edited 2020-12-18 09:51:39 +01:00 (CET)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.