Phenotype #0000174337

Individual ID	00233915
Associated disease	FDH
Phenotype details	dental defects; skin hypoplasia (HP:0008065); assymmetrical skeletal defects (HP:0011842); has oral features; coloboma (HP:0000589); microcephaly (HP:0000252);
Diagnosis/Initial	Goltz-Gorlin syndrome
Inheritance	Familial
Diagnosis/Definite	FDH
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Maria Paola Lombardi
Database submission license	No license selected
Created by	Maria Paola Lombardi
Date created	2010-03-18 15:03:45 +01:00 (CET)
Date last edited	2010-03-29 12:57:14 +02:00 (CEST)

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