21729-9LOINC 2.82
PSAP gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
PSAP gene Mut Anl Bld/T
Component
- PSAP gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; COLEC4; Genetics; GLBA; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Prosaposin; PSAP; PSPA; PSP-A; Random; SAP1; SFTP1; SFTPA1B; SPA; SP-A; SPA1; SP-A1; surfactant protein A1; Tissue; Tissue, unspecified; Variant Gaucher disease; Variant metachromatic leukodystrophy; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- COLEC4
- Genetics
- GLBA
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Prosaposin
- PSAP
- PSAP gene targeted mutation analysis
- PSP-A
- PSPA
- Random
- SAP1
- SFTP1
- SFTPA1B
- SP-A
- SP-A1
- SPA
- SPA1
- surfactant protein A1
- Tissue
- Tissue, unspecified
- Variant Gaucher disease
- Variant metachromatic leukodystrophy
- WB
- Whole blood
- Whole blood or Tissue