Phenotype #0000016071

Individual ID 00017745
Associated disease CISS
Phenotype details feeding problems (HP:0011968); camptodactyly (HP:0012385); poor swallowing (HP:0002015);
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination ?
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Insa Buers
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-09-18 19:38:23 +02:00 (CEST)
Date last edited 2020-04-07 11:38:19 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.