Phenotype #0000323651

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00433125
Associated disease	IMD
Phenotype details	neutrophil defect or congenital condition with bone marrow failure such as dyskeratosis congenita and Fanconi-like phenotype, anemia and thrombocytopenia
Diagnosis/Initial	primary immunodeficiency disease
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	6y (6 years)
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2023-02-28 15:41:53 +01:00 (CET)
Date last edited	N/A

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