Phenotype #0000344841
| Individual ID |
00456322 |
| Associated disease |
NDD |
| Diagnosis/Initial |
neurodevelopmental delay |
| Diagnosis/Definite |
DCIDP |
| Phenotype details |
developmental delay; speech delay; facial dysmorphism; intellectual disability; motor delay; MRI brain anomalies; skeletal malformations; hypotonia/abnormal tone; gastrointestinal problems; cardiac malformations; abnormal behavior; growth failure; hearing loss; feeding difficulties; microcephaly; no genital abnormalities; renal malformations; no seizures; no underweight; no short stature |
| Inheritance |
Isolated (sporadic) |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-10-24 11:13:35 +02:00 (CEST) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|