38922-1LOINC 2.82
PTCH gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
PTCH gene Mut Anl Bld/T
Component
- PTCH gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- BCNS; Blood; Genetics; Gorlin syndrome; Heredity; Heritable; HPE7; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NBCCS; Nevoid basal cell carcinoma syndrome; Nominal; Patched (Drosophila) homolog; patched 1; PCR; Point in time; PTC; PTC1; PTCH; PTCH11; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- BCNS
- Blood
- Genetics
- Gorlin syndrome
- Heredity
- Heritable
- HPE7
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- NBCCS
- Nevoid basal cell carcinoma syndrome
- Nominal
- Patched (Drosophila) homolog
- patched 1
- PCR
- Point in time
- PTC
- PTC1
- PTCH
- PTCH gene targeted mutation analysis
- PTCH11
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue