Phenotype #0000061048
| Individual ID |
00081462 |
| Associated disease |
ID |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Phenotype details |
Abnormality of the cardiovascular system (HP:0001626); Heart murmur (HP:0030148); Abnormality of male external genitalia (HP:0000032); Intellectual disability (HP:0001249); Delayed speech and language development (HP:0000750); Behavioral abnormality (HP:0000708); Autistic behavior (HP:0000729); intellectual disability (HP:0001249); no motor delay (-HP:0001270), delayed social development (HP:0012434); speech delay (HP:0000750) |
| Age/Examination |
14y08m (14 years, 8 months) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Sébastien Küry |
| Database submission license |
No license selected |
| Created by |
Sébastien Küry |
| Date created |
2016-10-14 10:35:24 +02:00 (CEST) |
| Date last edited |
2020-05-12 12:33:06 +02:00 (CEST) |
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