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239018005: Schoepf-Schulz-Passage syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
358197018 Schoepf-Schulz-Passage syndrome en Synonym Active Case sensitive SNOMED CT core
627977017 Schoepf-Schulz-Passage syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Schoepf-Schulz-Passage syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Occurrence Congenital true Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Schoepf-Schulz-Passage syndrome Finding site Ectoderm structure true Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Schoepf-Schulz-Passage syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Schoepf-Schulz-Passage syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 4
Schoepf-Schulz-Passage syndrome Finding site Hair structure true Inferred relationship Some 4
Schoepf-Schulz-Passage syndrome Occurrence Congenital true Inferred relationship Some 4
Schoepf-Schulz-Passage syndrome Finding site Nail unit structure true Inferred relationship Some 2
Schoepf-Schulz-Passage syndrome Finding site Tooth structure true Inferred relationship Some 3
Schoepf-Schulz-Passage syndrome Pathological process Pathological developmental process true Inferred relationship Some 4
Schoepf-Schulz-Passage syndrome Pathological process Pathological developmental process true Inferred relationship Some 3
Schoepf-Schulz-Passage syndrome Associated morphology Congenital anomaly false Inferred relationship Some
Schoepf-Schulz-Passage syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Finding site Skin structure false Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Finding site Skin structure false Inferred relationship Some 1
Schoepf-Schulz-Passage syndrome Finding site Skin structure false Inferred relationship Some 2
Schoepf-Schulz-Passage syndrome Occurrence Congenital true Inferred relationship Some 2
Schoepf-Schulz-Passage syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
Schoepf-Schulz-Passage syndrome Occurrence Congenital false Inferred relationship Some
Schoepf-Schulz-Passage syndrome Is a Ectodermal dysplasia with hair-tooth-nail defects true Inferred relationship Some
Schoepf-Schulz-Passage syndrome Occurrence Congenital true Inferred relationship Some 3
Schoepf-Schulz-Passage syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 3
Schoepf-Schulz-Passage syndrome Finding site Ectoderm structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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