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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