Phenotype #0000073516

Individual ID 00095121
Associated disease PTRPLS
Phenotype details intrauterine growth retardation (HP:0001511), hypertelorism (HP:0000316), ventriculomegaly (HP:0002119)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Karen Stals
Database submission license No license selected
Created by Karen Stals
Date created 2017-01-06 13:35:57 +01:00 (CET)
Date last edited 2017-01-08 13:02:52 +01:00 (CET)

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