Individual ID |
00219147 |
Associated disease |
ID |
Diagnosis/Initial |
intellectual disability |
Diagnosis/Definite |
MRX-102 |
Inheritance |
Unknown |
Phenotype details |
no decreased body weight (-HP:0004325); macrocephaly (HP:0000256); moderate intellectual disability (HP:0002342) ; hypotonia (HP:0001290); epilepsy (HP:0001250); movement disorder (incl. spasticity) (HP:0100022); abnormal behaviour (HP:0000708); skin abnormality (HP:0000951); hyperlaxity (HP:0001388); no visual problems (-HP:0000504); no hearing loss (-HP:0000365); no cleft lip or palate (-HP:0000202); no precocious puberty (-HP:0000826); no scoliosis (-HP:0002650) |
Age/Examination |
13y (13 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2019-02-06 21:03:42 +01:00 (CET) |
Date last edited |
2019-02-06 21:10:16 +01:00 (CET) |