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49013001: 17 alpha-Hydroxyprogesterone aldolase deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
81655014 17 alpha-Hydroxyprogesterone aldolase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
81656010 Steroid 17,20-lyase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
81657018 Male pseudohermaphroditism due to testicular 17,20-desmolase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
495287013 Defective synthesis of 17-20 desmolase en Synonym Active Entire term case insensitive SNOMED CT core module
786645016 17 alpha-Hydroxyprogesterone aldolase deficiency (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Enzymopathy true Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Hereditary disorder of endocrine system false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Reproductive system hereditary disorder false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Congenital adrenal hyperplasia - desmolase deficiency true Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Male pseudohermaphroditism false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Congenital anomaly of adrenal gland false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Entire genital organ false Inferred relationship Existential restriction modifier 3
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Course Multiple superficial injuries of lower leg false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Male structure false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 1
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Glandular hyperplasia false Inferred relationship Existential restriction modifier 1
17 alpha-Hydroxyprogesterone aldolase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 3
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Genital structure false Inferred relationship Existential restriction modifier 4
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Gonadal structure false Inferred relationship Existential restriction modifier 3
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Congenital anomaly of genital system false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Genital structure false Inferred relationship Existential restriction modifier 2
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 2
17 alpha-Hydroxyprogesterone aldolase deficiency Is a Congenital anomaly of adrenal gland false Inferred relationship Existential restriction modifier
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 1
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 3
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 1
17 alpha-Hydroxyprogesterone aldolase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier 3
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier 2
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 3
17 alpha-Hydroxyprogesterone aldolase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
17 alpha-Hydroxyprogesterone aldolase deficiency Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
17 alpha-Hydroxyprogesterone aldolase deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
46,XY disorder of sex development due to isolated 17,20-lyase deficiency Due to True 17 alpha-Hydroxyprogesterone aldolase deficiency Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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