Phenotype #0000269312

Individual ID 00373716
Associated disease CSS1;MRD12
Diagnosis/Initial -
Diagnosis/Definite Coffin-Siris syndrome 1 (OMIM 135900)
Phenotype details HP:0004322; HP:0001249; HP:0002750; HP:0001263; HP:0001999; HP:0009381
Inheritance Familial, autosomal dominant
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Wenjuan Qiu
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Wenjuan Qiu
Date created 2021-05-23 14:18:09 +02:00 (CEST)
Date last edited 2021-05-28 11:39:07 +02:00 (CEST)

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