Phenotype #0000326908

Individual ID 00436783
Associated disease FHL3
Phenotype details premature birth reduced hemoglobin, thrombocytopenia purpura ascites, splenomegaly
Diagnosis/Initial hemophagocytic syndrome
Inheritance Isolated (sporadic)
Diagnosis/Definite FHL3
Age/Examination 00y00m19d00h
Age/Diagnosis 00y02m09d00h
Age/Onset 00y00m19d00h
Phenotype/Onset -
Protein -
Owner name Yanhong Li
Database submission license No license selected
Created by Yanhong Li
Date created 2023-10-08 04:37:25 +02:00 (CEST)
Date last edited 2023-10-10 19:06:59 +02:00 (CEST)

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