SNOMED_CT

SNOMED CT Concept 722002002: Scholte syndrome

722002002 is a SNOMED CT concept used to represent Scholte 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 attributes19
Role groups6
Module900000000000207008
Parents12

Defining attributes

Associated morphologyDysplasia(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteBone structure of limb(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyAbsence(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteHair structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyMorphologically abnormal structure(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteFace structure(body structure)
Pathological processPathological developmental process(qualifier value)
OccurrenceCongenital(qualifier value)
Finding siteGonadal endocrine structure(body structure)
Pathological processPathological developmental process(qualifier value)
Has interpretationImpaired(qualifier value)
InterpretsIntellectual ability(observable entity)
Has interpretationImpaired(qualifier value)
InterpretsAdaptation behaviour(observable entity)

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

Intellectual disability, balding, patella luxation, acromicria syndromeScholte Begeer-van Essen syndrome

Frequently asked questions

Code details

Code722002002
SystemSNOMED_CT
Display nameScholte syndrome
DescriptionIntellectual disability, balding, patella luxation, acromicria 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 722002002 | Scholte syndrome | HealthAssure