Phenotype #0000325371

Individual ID 00435166
Associated disease GD1
Phenotype details I.13: splenomegaly, hepatomegaly, thrombocytopenia, cystalgia. I.30: splenomegaly, thrombocytopenia, leukopenia, chronic diarrhea, skin pigmentation. I.31:splenomegaly, hepatomegaly, thrombocytopenia, thrombocytopenia, leukopenia, stature and pubertal developmentdelayed, portal hypertension, irregularity of right humerus
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite GD1
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jimena Urbano
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Jimena Urbano
Date created 2023-06-01 17:01:24 +02:00 (CEST)
Date last edited 2023-10-27 15:19:23 +02:00 (CEST)

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