Phenotype #0000085713

Individual ID 00107961
Associated disease MTDPS13
Phenotype details SGA, FTT , Short stature, Microcephaly, Developmental delay, Hypotonia, White matter abnormalities, Lactate peak in MRS, Cardiomyopathy, , Feeding difficulties, Lactic acidemia, Prominent forehead
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 18:15:10 +02:00 (CEST)
Date last edited 2017-07-30 13:29:23 +02:00 (CEST)

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