DISEASES

Disease-gene associations mined from literature

Human genes for Scott syndrome

Scott syndrome [DOID:0111052]

An inherited blood coagulation disease characterized by autosomal recessive inheritance of hemorrhagic episodes due to impaired platelet coagulant activity that has material_basis_in homozygous mutation in the TMEM16F gene on chromosome 12q12.

Synonyms:  Scott syndrome,  DOID:0111052,  Scott disease,  Scott disorder,  Scott syndromes ...