Phenotype #0000025901

Individual ID	00032465
Associated disease	RIEG1
Phenotype details	no heart defect; no hearing loss; Hypertelorism, Meckel's diverticulum; umbilical hernia (HP:0001537); Axenfeld-Rieger syndrome; hypodontia, delayed eruption
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	2y (2 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 21:08:08 +01:00 (CET)
Date last edited	2025-02-03 11:32:17 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.