Global Variome shared LOVD

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Phenotype #0000222928 Individual ID 00289297 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Abnormality of globe location (HP:0100886); Arachnodactyly (HP:0001166); Abnormality of finger (HP:0001167); Defect in the atrial septum (HP:0001631); Dysphagia (HP:0002015); Abnormality of the esophagus (HP:0002031); Abnormality of the mandible (HP:0000277); Microretrognathia (HP:0000308); Abnormality of the nose (HP:0000366); Choanal stenosis (HP:0000452); Abnormality of the eye (HP:0000478); Abnormality of cardiac atrium (HP:0005120); Proptosis (HP:0000520); Abnormality of the clitoris (HP:0000056); Clitoral hypertrophy (HP:0008665); Abnormality of the skin (HP:0000951) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2020-03-02 12:27:04 +01:00 (CET) Date last edited 2020-04-02 12:33:15 +02:00 (CEST)

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