Human genes for Scott syndrome
Scott syndrome [DOID:0111052]
A 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 ...