Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation 1003438004

SNOMED CT code

SNOMED code

1003438004

name

Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation

status

active

date introduced

2021-01-31

fully specified name(s)

Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder)

synonyms

Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation
Leydig cell hypoplasia due to partial LH receptor inactivation

attributes - group1

Finding site

Structure of interstitial cell of Leydig 44185004

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Associated morphology

Hypoplasia 55199003

parents

Leydig cell agenesis 56212008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of connective tissue 105969002
Congenital connective tissue disorder 363039000
Leydig cell agenesis 56212008
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation 1003438004

ancestors

sorted most to least specific

Leydig cell agenesis 56212008
Congenital connective tissue disorder 363039000
Connective tissue hereditary disorder 363045008
Developmental hereditary disorder 363070008
Hereditary disorder of endocrine system 363104002
Reproductive system hereditary disorder 363290007
Congenital anomaly of endocrine testis 371122009
Congenital hypoplasia of testis 85437001
Autosomal recessive hereditary disorder 85995004
Disorder of connective tissue 105969002
Congenital anomaly of endocrine gonad 371118004
Congenital hypoplasia of testis and scrotum 15965901000119108
Autosomal hereditary disorder 1899006
Hereditary disorder by system 363137000
Congenital anomaly of testis 55631001
Disorder of endocrine testis 73820008
Congenital hypoplasia of gonad 93261006
Hereditary disease 32895009
Disorder of endocrine gonad 127345001
Congenital anomaly of male genital system 4406004
Gonadal dysgenesis 205681004
Congenital anomaly of endocrine gland 4184009
Disorder of testis 64910008
Genetic disease 782964007
Disorder of endocrine system 362969004
Congenital malformation of genital organs 204821009
Congenital anomaly of male urogenital tract 428522008
Disorder of male genital organ 64557000
Testicular finding 249236000
Genitourinary congenital anomalies 287085006
Disorder of male reproductive system 363194005
Disorder of reproductive system 362968007
Congenital anomaly of lower trunk 363030001
Male genitalia finding 249230006
Disorder of pelvic region of trunk 609619005
Disorder of the genitourinary system 42030000
Genital finding 300479008
Congenital abnormality of lower limb and pelvic girdle 253937004
Congenital anomaly of trunk 78626001
Finding of pelvic region of trunk 609625009
Disorder of body system 362965005
Urogenital finding 118238000
Congenital malformation 276654001
Disorder of abdominopelvic segment of trunk 822988000
Finding of abdominopelvic segment of trunk 822987005
Developmental disorder 5294002
Congenital disease 66091009
Disorder of trunk 128121009
Disease 64572001
Finding of trunk structure 302292003
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Disorder of connective tissue 105969002

Congenital connective tissue disorder 363039000

Leydig cell agenesis 56212008

Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation 1003438004

SNOMED CT code