21700-0LOINC 2.82
Kallmann syndrome gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
KMS gene Mut Anl Bld/T
Component
- Kallmann syndrome gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Adhesion molecule-like, X-linked, ADMLX, anosmin 1; Anosmic hypogonadism; Blood; Dysplasia olfactogenitalis of de Morsier; Genetics; Heredity; Heritable; HHA; Hypogonadotropic hypogonadism and anosmia; Identity or presence; Inherited; KMS; KMS gene; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Adhesion molecule-like, X-linked, ADMLX, anosmin 1
- Anosmic hypogonadism
- Blood
- Dysplasia olfactogenitalis of de Morsier
- Genetics
- Heredity
- Heritable
- HHA
- Hypogonadotropic hypogonadism and anosmia
- Identity or presence
- Inherited
- Kallmann syndrome gene targeted mutation analysis
- KMS
- KMS gene
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue