Phenotype #0000180299

Individual ID 00240147
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details see paper; ..., albinism, delayed myelination, delayed development, organomegaly, hypopigmentation, no osteopetrosis
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-06-11 17:09:04 +02:00 (CEST)
Date last edited 2019-06-11 17:10:50 +02:00 (CEST)

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