Microphthalmos

Preferred Label : Microphthalmos;

Inclusion CIM-10 : Dysplasia of eye; Cryptophthalmos NOS; Hypoplasia of eye; Rudimentary eye;

ICD-10 exclusion note : cryptophthalmos syndrome (Q87.0);

Diag associé à un acte (%) : 92.4;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q112;

UMLS CUI

C0026010;

Automatic exact mappings (from CISMeF team)
- Cryptophthalmia [ICD-11 Sub-sub category]
- Dysplasia of eye (disorder) [SNOMED CT concept]
- Hypoplasia of eye (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- MICROPHTHALMOS [WHO-ART Included Term]
- Microphthalmia [MedDRA LLT]
- Microphthalmia [PASCAL descriptor]
- Microphthalmia [HPO term]
- Microphthalmos [MedDRA Preferred Term]
- Microphthalmos [NCIt concept]
- Microphthalmos [ICD-11 Subcategory]
- Microphthalmos (disorder) [SNOMED CT concept]
- microphthalmia [Disease (Nov.)]
- microphthalmia [DO Concept]
- microphthalmos [MeSH concept]
- microphthalmos [MeSH Descriptor]
- microphthalmos, nos [SNOMED Notion]
DO Cross reference
- cryptophthalmia [DO Concept]
- microphthalmia [DO Concept]
Excluded by
- Congenital malformations of eyelid, lacrimal apparatus and orbit [ICD-10 category]
ICD-10 exclusion(s)
- Congenital malformation syndromes predominantly affecting facial appearance [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Isolated cryptophthalmia [ORDO Disease]
Orphanet concepts
- Colobomatous microphthalmia [ORDO Disease]
- Complete cryptophthalmia [ORDO Disease]
- Congenital symblepharon [ORDO Disease]
- Isolated cryptophthalmia [ORDO Disease]
- Isolated microphthalmia-anophthalmia-coloboma [ORDO Disease]
- Matthew-Wood syndrome [ORDO Disease]
- Microphthalmia with brain and digit anomalies [ORDO Disease]
- Microphthalmia with linear skin defects syndrome [ORDO Disease]
- Microphthalmia, Lenz type [ORDO Disease]
- Microphthalmia-ankyloblepharon-intellectual disability syndrome [ORDO Disease]
- Microphthalmia-anophthalmia-coloboma [ORDO Disease]
- Microphthalmia-brain atrophy syndrome [ORDO Disease]
- Nanophthalmos [ORDO Disease]
- Partial cryptophthalmia [ORDO Disease]
- Syndromic microphthalmia type 5 [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital microphthalmos [MedDRA LLT]
- MICROPHTHALMOS [WHO-ART Included Term]
- Microphthalmia [MedDRA LLT]
- Microphthalmia [HPO term]
- Microphthalmia [PASCAL descriptor]
- Microphthalmos [MedDRA Preferred Term]
- Microphthalmos [ICD-9 code]
- Microphthalmos [NCIt concept]
- Microphthalmos [ICD-11 Subcategory]
- Microphthalmos (disorder) [SNOMED CT concept]
- Microphthalmos, unspecified [MedDRA LLT]
- Microphthalmos, unspecified [ICD-9 code]
- Simple microphthalmos [MedDRA LLT]
- Simple microphthalmos [ICD-9 code]
- Simple microphthalmos (disorder) [SNOMED CT concept]
- microphthalmia [DO Concept]
- microphthalmia [Disease (Nov.)]
- microphthalmos [MeSH Descriptor]
- microphthalmos [MeSH concept]
- microphthalmos, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients