Phenotype #0000025889

Individual ID 00032453
Associated disease RIEG1
Phenotype details no heart defect; no hearing loss; ankyloglossia; redundant umbilical skin; umbilical hernia (HP:0001537); Axenfeld-Rieger syndrome, microcornea; microdontia, dental anomaly
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite -
Age/Examination 1y6m (1 year, 6 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Elena Semina
Database submission license No license selected
Created by Elena Semina
Date created 2012-02-19 20:37:59 +01:00 (CET)
Date last edited 2025-02-03 11:32:17 +01:00 (CET)

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