FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

279923002: Tubule of paroophoron (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
417386013 Tubule of paroophoron en Synonym Active Case insensitive SNOMED CT core
673272017 Tubule of paroophoron (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Tubule of paroophoron Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Tubule of paroophoron Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
Tubule of paroophoron Pathological process Pathological developmental process true Inferred relationship Some 1
Tubule of paroophoron Pathological process Pathological developmental process false Inferred relationship Some 2
Tubule of paroophoron Finding site Paroophoron true Inferred relationship Some 1
Tubule of paroophoron Associated morphology Persistent embryonic structure true Inferred relationship Some 1
Tubule of paroophoron Associated morphology Congenital anomaly false Inferred relationship Some 1
Tubule of paroophoron Finding site Genital structure false Inferred relationship Some 4
Tubule of paroophoron Is a Congenital anomaly of endocrine gonad false Inferred relationship Some
Tubule of paroophoron Finding site Female genital tract false Inferred relationship Some
Tubule of paroophoron Is a Congenital anomaly of endocrine ovary false Inferred relationship Some
Tubule of paroophoron Finding site Genital structure false Inferred relationship Some 2
Tubule of paroophoron Associated morphology Congenital malformation false Inferred relationship Some 2
Tubule of paroophoron Is a Congenital anomaly of ovary false Inferred relationship Some
Tubule of paroophoron Is a Congenital anomaly of endocrine gland false Inferred relationship Some
Tubule of paroophoron Finding site Ovarian endocrine structure false Inferred relationship Some 1
Tubule of paroophoron Is a Congenital anomaly of abdomen false Inferred relationship Some
Tubule of paroophoron Is a Congenital anomaly of body cavity false Inferred relationship Some
Tubule of paroophoron Is a Congenital anomaly of female genital system false Inferred relationship Some
Tubule of paroophoron Associated morphology Congenital anomaly false Inferred relationship Some 1
Tubule of paroophoron Finding site Ovarian endocrine structure false Inferred relationship Some 1
Tubule of paroophoron Is a Congenital anomaly of the pelvis false Inferred relationship Some
Tubule of paroophoron Is a Paroophoron true Inferred relationship Some
Tubule of paroophoron Associated morphology Congenital anomaly false Inferred relationship Some 2
Tubule of paroophoron Finding site Paroophoron false Inferred relationship Some 2
Tubule of paroophoron Occurrence Congenital true Inferred relationship Some 1
Tubule of paroophoron Associated morphology Developmental abnormality false Inferred relationship Some 1
Tubule of paroophoron Finding site Female genital structure false Inferred relationship Some 1
Tubule of paroophoron Occurrence Congenital false Inferred relationship Some
Tubule of paroophoron Finding site Entire genital organ false Inferred relationship Some 2
Tubule of paroophoron Associated morphology Developmental abnormality false Inferred relationship Some 2
Tubule of paroophoron Course Multiple superficial injuries of lower leg false Inferred relationship Some
Tubule of paroophoron Finding site Entire endocrine ovary false Inferred relationship Some 1
Tubule of paroophoron Is a Congenital anomaly of female genital system false Inferred relationship Some
Tubule of paroophoron Is a Residual ovary syndrome false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start