Phenotype #0000199679
| Individual ID |
00261173 |
| Associated disease |
DD |
| Phenotype details |
developmental delay/intellectual disability (HP:0012758/HP:0001249); autism spectrum disorder (HP:0000729); attention deficit hyperactivity disorder (HP:0007018); no stereotypic behavior (-HP:0000733); no seizures (-HP:0001250); muscular hypotonia (HP:0001252); no ataxia (-HP:0001251); no abnormal prenatal brain imaging; microcephaly (HP:0000252); no macrocephaly (-HP:0000256); facial dysmorphism (HP:0000271); small joint hypermobility |
| Diagnosis/Initial |
developmental delay |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
9y (9 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 |
2019-08-11 12:19:47 +02:00 (CEST) |
| Date last edited |
N/A |
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