Phenotype #0000199533

Individual ID 00261001
Associated disease IMD30
Phenotype details IMD30, IL12RB1 deficiency, MSMD
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license No license selected
Created by Esther van de Vosse
Date created 2017-07-31 16:22:12 +02:00 (CEST)
Date last edited N/A

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