Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000174434 Individual ID 00234012 Associated disease FDH Phenotype details only cutaneous symptoms present; skin hypoplasia (HP:0008065); no syndactyly (-HP:0001159), no polydactyly (-HP:0010442); no oligodontia (-HP:0000677); no microphthalmia (-HP:0000568); no displaced anus (-HP:0004397); no osteopathia striata (-HP:001074), no omphalocele (-HP:0001539) Diagnosis/Initial focal dermal hypoplasia Inheritance Unknown 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 14:49:46 +01:00 (CET) Date last edited 2013-12-27 14:55:52 +01:00 (CET)

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