77057-8LOINC 2.82
CYP17A1 gene full mutation analysis in Blood or Tissue by Sequencing
CYP17A1 Full Mut Anl Bld/T Seq
Component
- CYP17A1 gene full mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Sequencing
Related names
- 17-alpha-hydroxylase/17,20-lyase deficiency; Adrenal hyperplasia; Blood; CPT7; CYP17; cytochrome P450, family 17, subfamily A, polypeptide 1; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; P450C17; Point in time; Pseudohermaphroditism; Random; S17AH; sequencing of entire coding region; Steroid-17 alpha-hydroxylase deficiency; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- 17-alpha-hydroxylase/17,20-lyase deficiency
- Adrenal hyperplasia
- Blood
- CPT7
- CYP17
- cytochrome P450, family 17, subfamily A, polypeptide 1
- Document
- Finding
- Findings
- full gene sequencing
- Full Mut Anl
- Genetics
- Heredity
- Heritable
- high-throughput sequencing
- HTS
- Inherited
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutations
- Next generation sequencing
- NGS
- P450C17
- Point in time
- Pseudohermaphroditism
- Random
- S17AH
- sequencing of entire coding region
- Steroid-17 alpha-hydroxylase deficiency
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue