41109-0LOINC 2.82
FGD1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
FGD1 gene Mut Anl Bld/T
Component
- FGD1 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- AAS; Blood; Faciogenital dysplasia (Aarskog-Scott syndrome); FGDY; FYVE, RhoGEF and PH domain containing 1; FYVE, RhoGEF and PH domain containing 1 (faciogenital dysplasia); Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRXS16; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; ZFYVE3
Index terms
- AAS
- Blood
- Faciogenital dysplasia (Aarskog-Scott syndrome)
- FGD1 gene targeted mutation analysis
- FGDY
- FYVE, RhoGEF and PH domain containing 1
- FYVE, RhoGEF and PH domain containing 1 (faciogenital dysplasia)
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MRXS16
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue
- ZFYVE3