Phenotype #0000125487

Individual ID 00152125
Associated disease CPCMR
Diagnosis/Initial -
Diagnosis/Definite MEIS2-related syndrome
Phenotype details Tetralogy of Fallot (HP:0001636); Ebstein's malformation (HP:0010316); feeding difficulties (HP:0011968); strabismus (HP:0025068); scoliosis (HP:0002650); learning problems (HP:0001328)
Inheritance Familial, autosomal dominant
Age/Examination 18y03m (18 years, 3 months)
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jeroen Breckpot
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Jeroen Breckpot
Date created 2018-02-02 11:47:30 +01:00 (CET)
Date last edited N/A

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