Phenotype #0000174436

Individual ID 00234014
Associated disease FDH
Phenotype details absent L arm and L leg, asymmetric ventriculomegaly, absent corpus callosum,typeII Chiari malformation, cleft lip/palate, open neural tube defect, ventricular wall defect, stomach absent; no oligodactyly (-HP:0012165); kidney malformation (HP:0012210), heart defect (HP:0001627);
Diagnosis/Initial focal dermal hypoplasia
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 2013-12-27 15:57:23 +01:00 (CET)
Date last edited 2014-01-10 23:31:48 +01:00 (CET)

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