Phenotype #0000179401

Individual ID 00239179
Associated disease FDH
Phenotype details L>R facial asymmetry, hyperpigmentation, fat deposits, skin atrophy, R hand syndactyly, L foot ectrodactyly, L foot syndactyly, long bone reduction, limb defects
Diagnosis/Initial FDH
Inheritance Familial, X-linked dominant
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 2019-06-04 14:17:00 +02:00 (CEST)
Date last edited N/A

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