SNOMED_CT

SNOMED CT Concept 1332382002: COMMAD syndrome

1332382002 is a SNOMED CT concept used to represent COMMAD 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 attributes37
Role groups12
Module900000000000207008
Parents12

Defining attributes

Associated morphologyAbnormal smallness(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteEntire eye proper(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyDevelopmental failure of fusion(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteEye structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyDecreased melanin pigmentation(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteSkin structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyDecreased melanin pigmentation(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteEye structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyEnlargement(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteHead structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyMorphologically abnormal structure(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteBone structure(body structure)
Pathological processPathological developmental process(qualifier value)
Associated morphologyHypoplasia(morphologic abnormality)
OccurrenceCongenital(qualifier value)
Finding siteOptic nerve structure(body structure)
Pathological processPathological developmental process(qualifier value)
OccurrenceCongenital(qualifier value)
Finding siteStructure of auditory system(body structure)
Has interpretationDecreased(qualifier value)
InterpretsHearing(observable entity)
Has interpretationBelow reference range(qualifier value)
InterpretsOsteoclast turnover rate(observable entity)
Has interpretationAbove reference range(qualifier value)
InterpretsHead circumference(observable entity)
Clinical courseProgressive(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

COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndromeColoboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome

Frequently asked questions

Code details

Code1332382002
SystemSNOMED_CT
Display nameCOMMAD syndrome
DescriptionColoboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness 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 1332382002 | COMMAD syndrome | HealthAssure