Phenotype #0000025896

Individual ID	00032460
Associated disease	RIEG1
Phenotype details	no heart defect; no hearing loss; maxillary hypoplasia, Imperforate anus, thin upper lip; redundant umbilical skin; Axenfeld-Rieger syndrome, aniso-metropia; hypodontia, microdontia
Diagnosis/Initial	-
Inheritance	Familial
Diagnosis/Definite	-
Age/Examination	13y (13 years)
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 20:50:48 +01:00 (CET)
Date last edited	2025-02-03 11:32:17 +01:00 (CET)

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