Phenotype #0000155191
| Individual ID |
00207418 |
| Associated disease |
LS |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Initial |
- |
| Age/Examination |
- |
| Diagnosis/Definite |
- |
| Age/Diagnosis |
- |
| Age/Onset |
00y04m |
| Phenotype/Onset |
- |
| Phenotype details |
Leigh-like, profound global developmental delay(HP:0001263), hypotonia and seizures (HP:0001250) |
| Protein |
- |
| Owner name |
Sze Chern Lim |
| Database submission license |
No license selected |
| Created by |
Sze Chern Lim |
| Date created |
2018-11-22 07:24:48 +01:00 (CET) |
| Date last edited |
2018-11-22 09:24:21 +01:00 (CET) |
|