Phenotype #0000085707

Global Variome shared LOVD

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

Individual ID	00107956
Associated disease	MTDPS13
Phenotype details	FTT , Short stature, Microcephaly, Developmental delay, Hypotonia, Arrhythmia, Feeding difficulties, Lactic acidemia
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Hongzheng Dai
Database submission license	No license selected
Created by	Hongzheng Dai
Date created	2017-07-20 16:21:20 +02:00 (CEST)
Date last edited	2017-07-30 13:29:23 +02:00 (CEST)

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