FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

239018005: Schoepf-Schulz-Passage syndrome (disorder)


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

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Schoepf-Schulz-Passage syndrome Is a Ectodermal dysplasia with hair-tooth-nail defects true Inferred relationship Some
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 Occurrence Congenital false Inferred relationship Some
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 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 anomaly false Inferred relationship Some 2
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
Schoepf-Schulz-Passage syndrome Pathological process (attribute) 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 (attribute) 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 (morphologic abnormality) true Inferred relationship Some 2
Schoepf-Schulz-Passage syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Schoepf-Schulz-Passage syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Schoepf-Schulz-Passage syndrome Finding site Hair structure (body 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 (attribute) Pathological developmental process true Inferred relationship Some 4
Schoepf-Schulz-Passage syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start