35744-2LOINC 2.82
TP73L gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
TP73L gene Mut Anl Bld/T
Component
- TP73L gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- AIS; B(p51A); B(p51B); Blood; Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome; EEC dysplasia; EEC3; Genetics; Heredity; Heritable; HGNC:15979; Identity or presence; Inherited; KET; LMS; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NBP; Nominal; OFC8; p40; p51; p53CP; p63; p73H; p73L; PCR; Point in time; Random; RHS; SHFM4; Tissue; Tissue, unspecified; TP53CP; TP53L; TP63; TP73L; Tumor protein 63 kDa with strong homology to p53 gene; tumor protein p63; Tumor protein p73-like gene; WB; Whole blood; Whole blood or Tissue
Index terms
- AIS
- B(p51A)
- B(p51B)
- Blood
- Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome
- EEC dysplasia
- EEC3
- Genetics
- Heredity
- Heritable
- HGNC:15979
- Identity or presence
- Inherited
- KET
- LMS
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- NBP
- Nominal
- OFC8
- p40
- p51
- p53CP
- p63
- p73H
- p73L
- PCR
- Point in time
- Random
- RHS
- SHFM4
- Tissue
- Tissue, unspecified
- TP53CP
- TP53L
9 further terms