Phenotype #0000232906
Individual ID |
00307087 |
Associated disease |
HSCR1 |
Phenotype details |
HP:0002251 |
Diagnosis/Initial |
Hirschsprung disease |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
HSCR1 |
Age/Examination |
01y (1 year) |
Age/Diagnosis |
15y |
Age/Onset |
01y |
Phenotype/Onset |
HP:0002251 |
Protein |
- |
Owner name |
A. Arteche-López |
Database submission license |
No license selected |
Created by |
A. Arteche-López |
Date created |
2020-07-30 19:08:35 +02:00 (CEST) |
Date last edited |
2020-07-31 12:29:04 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|