SNOMED_CT

SNOMED CT Concept 700062000: Schöpf-Schulz-Passarge syndrome

700062000 is a SNOMED CT concept used to represent Schöpf-Schulz-Passarge syndrome in structured clinical data. You may see this concept in clinical documentation systems, problem lists, terminology services, interoperability records, or semantic mapping workflows. SNOMED CT is a clinical terminology used to capture healthcare meaning in a standardized, interoperable form. This concept is typed as a disorder in the terminology hierarchy.

Reviewed by HealthAssure Clinical TeamUpdated 26 May 2026

What is this code?

SNOMED CT is a clinical terminology used to capture healthcare meaning in a standardized, interoperable form. This concept is typed as a disorder in the terminology hierarchy.

When is it used?

  • Used to represent a standardized clinical concept in health records, terminology services, and semantic mappings.
  • Often linked to diagnoses, findings, procedures, body structures, organisms, substances, or observable entities depending on the concept type.
  • Semantic tag: disorder

What it does not mean

  • A terminology concept label alone does not replace clinical interpretation, diagnosis context, or treatment advice.

Key facts

Semantic tagDisorder
Definition statusPrimitive
Definition patternSubclass
OWL axioms1
Defining attributes25
Role groups8
Module900000000000207008
Parents12

Defining attributes

Associated morphologyMultiple cysts(morphologic abnormality)
Finding siteEyelid structure(body structure)
Associated morphologyAbnormal number(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteTooth structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyDysplasia(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteEctoderm structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyHyperkeratosis(morphologic abnormality)
Finding siteEntire skin of palmar area of hand(body structure)
Associated morphologyHyperkeratosis(morphologic abnormality)
Finding siteEntire skin of sole of foot(body structure)
Associated morphologyAbsence(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteTooth structure(body structure)
Associated morphologyDystrophy(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteNail unit structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyGrowth alteration(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteHair structure(body structure)
Pathological processPathological developmental process(qualifier value)

Where you may see this code

You may see this concept in clinical documentation systems, problem lists, terminology services, interoperability records, or semantic mapping workflows.

Common synonyms

Keratosis palmoplantaris, cystic eyelids, hypodontia, hypotrichosis syndromeEccrine tumours ectodermal dysplasiaSSPS - Schöpf Schulz Passarge syndromeEccrine tumors ectodermal dysplasiaPalmoplantar hyperkeratosis, cystic eyelids, hypodontia, hypotrichosis syndromePalmoplantar keratoderma, cystic eyelids, hypodontia, hypotrichosis syndromeSchöpf Schulz Passarge syndrome

Frequently asked questions

Code details

Code700062000
SystemSNOMED_CT
Display nameSchöpf-Schulz-Passarge syndrome
DescriptionSchöpf-Schulz-Passarge syndrome (disorder)

Flags

BillableNo
Valid clinical useNo

Source

SourceSNOMED CT
Version20260501T120000Z
Releasesnapshot

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from SNOMED CT. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.

SNOMED CT 700062000 | Schöpf-Schulz-Passarge syndrome | HealthAssure