Phenotype #0000054385
| Individual ID |
00074629 |
| Associated disease |
ID |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Familial, X-linked recessive |
| Phenotype details |
long face (HP:0000276), short columella (HP:0002000), long philtrum (HP:0000343), thin upper lip vermilion (HP:0000219), wide mouth (HP:0000154), micrognathia (HP:0000347), hypotonic face (HP:0000271); intellectual disability (HP:0001249); global developmental delay (HP:0001263) |
| Age/Examination |
12y08m (12 years, 8 months) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Pieter Klap |
| Database submission license |
No license selected |
| Created by |
Pieter Klap |
| Date created |
2016-07-11 15:28:39 +02:00 (CEST) |
| Date last edited |
2020-05-12 12:33:06 +02:00 (CEST) |
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