53883-5LOINC 2.82
OCRL1 mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
OCRL1 gene Mut Anl Bld/T
Component
- OCRL1 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; INPP5F; LOCR; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; NPHL2; OCRL1; OCRL-1; oculocerebrorenal syndrome of Lowe; ovarian cancer-related protein 1; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- INPP5F
- LOCR
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- NPHL2
- OCRL-1
- OCRL1
- OCRL1 gene targeted mutation analysis
- oculocerebrorenal syndrome of Lowe
- ovarian cancer-related protein 1
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue