Phenotype #0000291061
Individual ID |
00397932 |
Associated disease |
WABS |
Diagnosis/Initial |
Warsaw breakage syndrome |
Diagnosis/Definite |
WABS |
Phenotype details |
no family history miscarriages; microcephaly; sensorineural hearing loss; prenatal growth restriction; postnatal growth restriction; intellectual disability; retrognathia; sloping/small forehead; no clinodactily; no bulbous nose; small nares; short neck; no syndactyly; tetraology of Fallot |
Inheritance |
Familial, autosomal recessive |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Johan den Dunnen |
Database submission license |
No license selected |
Created by |
Johan den Dunnen |
Date created |
2021-12-29 17:07:09 +01:00 (CET) |
Date last edited |
2021-12-29 17:17:55 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|