Hyperpigmentation of eyelids

Preferred Label : Hyperpigmentation of eyelids;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %145100;

Détails

Origin ID

145100;

UMLS CUI

C0155211;

Automatic exact mappings (from CISMeF team)
- Hyperpigmentation of eyelid [ICD-9 code]
- hyperpigmentation of eyelid [DO Concept]
Currated CISMeF NLP mapping
- Hyperpigmentation of eyelid [MedDRA LLT]
- Hyperpigmentation of eyelid (disorder) [SNOMED CT concept]
- Hyperpigmentation of eyelids [HPO term]
- hyperpigmentation of eyelid, nos [SNOMED Notion]
- hyperpigmentation of eyelids [MeSH concept]
- hyperpigmentation of eyelids [MeSH Supplementary Concept]
DO Cross reference
- hyperpigmentation of eyelid [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hyperpigmentation of eyelids [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperpigmentation of eyelid [MedDRA LLT]
- Hyperpigmentation of eyelid [ICD-9 code]
- Hyperpigmentation of eyelid (disorder) [SNOMED CT concept]
- Hyperpigmentation of eyelids [HPO term]
- hyperpigmentation of eyelid [DO Concept]
- hyperpigmentation of eyelid, nos [SNOMED Notion]
- hyperpigmentation of eyelids [MeSH Supplementary Concept]
- hyperpigmentation of eyelids [MeSH concept]

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