Phenotype #0000174435

Individual ID 00234013
Associated disease FDH
Phenotype details mild asymmetry of of ears, mildly short palpebral fissures; nail dysplasia (HP:0002164), skin hypoplasia (HP:0008065); no syndactyly (-HP:0001159), no polydactyly (-HP:0010442), no ectrodactyly (-HP:0100257); oligodontia (HP:0000677); no coloboma (-HP:0000589); no hydronephrosis (-HP:0000126), 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 15:26:24 +01:00 (CET)
Date last edited 2014-01-10 23:29:07 +01:00 (CET)

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