Phenotype #0000236886

Individual ID 00311633
Associated disease VWD
Inheritance Familial, autosomal recessive
Diagnosis/Initial VWD
Protein VWF_Ag:<3 , FVIII_C:1.9
Diagnosis/Definite VWD3
Protein/Multimer_profile -
BleedingScore -
BleedingScore/Tool -
Phenotype details menorrhagia, muscle haematomas, CNS bleeding
Owner name Hamideh Yadegari