Leydig cell agenesis 56212008
SNOMED CT code
SNOMED code | 56212008 |
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name | Leydig cell agenesis |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Leydig cell agenesis (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Hypoplasia 55199003 |
Finding site | Structure of interstitial cell of Leydig 44185004 |
Occurrence | Congenital 255399007 |
parents |
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children |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 Leydig cell agenesis 56212008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Leydig cell agenesis 56212008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Leydig cell agenesis 56212008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Leydig cell agenesis 56212008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Leydig cell agenesis 56212008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital anomaly of endocrine gland 4184009 Congenital anomaly of endocrine gonad 371118004 Congenital anomaly of endocrine testis 371122009 Leydig cell agenesis 56212008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of trunk structure 302292003 Finding of abdominopelvic segment of trunk 822987005 Urogenital finding 118238000 Genital finding 300479008 Congenital malformation of genital organs 204821009 Congenital anomaly of male genital system 4406004 Congenital hypoplasia of testis and scrotum 15965901000119108 Congenital hypoplasia of testis 85437001 Leydig cell agenesis 56212008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Leydig cell agenesis 56212008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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