77058-6LOINC 2.82
CYP17A1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
CYP17A1 Fam Mut Anl Bld/T
Component
- CYP17A1 gene mutation analysis limited to known familial mutations
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- 17-alpha-hydroxylase/17,20-lyase deficiency; Adrenal hyperplasia; Blood; CPT7; CYP17; cytochrome P450, family 17, subfamily A, polypeptide 1; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; P450C17; PCR; Point in time; Pseudohermaphroditism; Random; S17AH; 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
- Fam Mut Anl
- Finding
- Findings
- Genetics
- Heredity
- Heritable
- Inherited
- LMTED
- LTD
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutation
- Mutations
- Muts
- P450C17
- PCR
- Point in time
- Pseudohermaphroditism
- Random
- S17AH
- Steroid-17 alpha-hydroxylase deficiency
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue