Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007
SNOMED CT code
| SNOMED code | 782917007 |
|---|---|
| name | Familial adrenal hypoplasia with absent pituitary luteinizing hormone |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Familial adrenal hypoplasia with absent pituitary luteinizing hormone (disorder) |
| synonyms |
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| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Gonadal endocrine structure 304041004 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of distal part of pituitary 52618001 |
| attributes - group4 | |
| Interprets | Luteinizing hormone measurement 69527006 |
| Has interpretation | Absent 2667000 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hypoplasia 55199003 |
| Finding site | Adrenal cortex structure 68594002 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group5 | |
| Interprets | Endocrine observable 364387009 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 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 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Procedure related finding 127325009 Evaluation finding 441742003 Measurement finding 118245000 Finding of substance level 785671009 Hormone level - finding 365774006 Gonadotrophin level - finding 365779001 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Endocrine finding 106176003 Hormone abnormality 84452004 Abnormal pituitary luteinizing hormone 386776005 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Procedure related finding 127325009 Evaluation finding 441742003 Measurement finding 118245000 Measurement procedure result absent 442228008 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hypogonadotropic hypogonadism 722944006 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Congenital anomaly of adrenal gland 60637003 Congenital hypoplasia of adrenal gland 93235007 Familial adrenal hypoplasia with absent pituitary luteinizing hormone 782917007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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