Phenotype #0000125485

Individual ID 00152123
Associated disease CPCMR
Diagnosis/Initial -
Diagnosis/Definite MEIS2-related syndrome
Phenotype details bifid uvula (HP:0000193); broad forehead (HP:0000337); medial flaring of eyebrows (HP:0010747); hypertelorism (HP:0000316); distichiasis (HP:0009743); thin upper lip (HP:0000219); beaked nose (HP:0003683); retrognathia (HP:0000278); intellectual disability, mild (HP:0001256); cryptorchidism (HP:0000028); iris nevus (HP:0011525); precocious puberty (HP:0008185); scoliosis (HP:0002650)
Inheritance Familial, autosomal dominant
Age/Examination -
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 11:31:39 +01:00 (CET)
Date last edited N/A

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