Phenotype #0000085717

Individual ID 00107966
Associated disease MTDPS13
Phenotype details White matter abnormalities, Cerebral atrophy, Peri/paraventricualr cysts, Hydrocephalus/ dilated ventricles, Brain stem atrophy, Lactate peak in MRS, Cardiomyopathy, Congenital heart disease, , Feeding difficulties, Lactic acidemia, Hyperammonemia
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 18:41:23 +02:00 (CEST)
Date last edited 2017-07-30 13:29:23 +02:00 (CEST)

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