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93131008: Leptocephaly (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
154076014 Leptocephaly en Synonym Active Case insensitive SNOMED CT core
154077017 Leptocephalus en Synonym Active Case insensitive SNOMED CT core
836801018 Leptocephaly (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
Leptocephaly Occurrence Congenital true Inferred relationship Some 1
Leptocephaly Pathological process Pathological developmental process true Inferred relationship Some 1
Leptocephaly Associated morphology Abnormal shape true Inferred relationship Some 1
Leptocephaly Is a Congenital anomaly false Inferred relationship Some
Leptocephaly Is a Congenital abnormality of skull shape true Inferred relationship Some
Leptocephaly Associated morphology Congenital abnormal shape false Inferred relationship Some 1
Leptocephaly Finding site Bone structure of cranium false Inferred relationship Some 1
Leptocephaly Occurrence Congenital false Inferred relationship Some 2
Leptocephaly Finding site Bone structure of cranium false Inferred relationship Some 2
Leptocephaly Associated morphology Congenital abnormal shape false Inferred relationship Some 2
Leptocephaly Finding site Bone structure of cranium true Inferred relationship Some 1
Leptocephaly Associated morphology Congenital abnormal shape false Inferred relationship Some 1
Leptocephaly Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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