Macules, hereditary congenital hypopigmented and hyperpigmented

Preferred Label : Macules, hereditary congenital hypopigmented and hyperpigmented;

Obsolete resource : true;

Moved to : 145250;

Inheritance : Autosomal dominant;

Prefixed ID : 154000;

Details

Origin ID

154000;

UMLS CUI

C1835172;

Currated CISMeF NLP mapping
- Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome (disorder) [SNOMED CT concept]
- Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome [ORDO Disease]
- Macules hereditary congenital hypopigmented and hyperpigmented [MeSH concept]
- macules hereditary congenital hypopigmented and hyperpigmented [MeSH Supplementary Concept]
HPO term(s)
- macules [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome (disorder) [SNOMED CT concept]
- Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome [ORDO Disease]
- Macules hereditary congenital hypopigmented and hyperpigmented [MeSH concept]
- macules hereditary congenital hypopigmented and hyperpigmented [MeSH Supplementary Concept]

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