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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
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| Preferred Name | Dyschromatosis Universalis Hereditaria | |
| Synonyms |
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| Definitions |
A genetically heterogenous condition, usually inherited in an autosomal dominant fashion, characterized by hypopigmented and hyperpigmented macules involving the entire body surface. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C173131 |
|
| code |
C173131
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| Contributing_Source |
Cellosaurus
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|
| definition |
A genetically heterogenous condition, usually inherited in an autosomal dominant fashion, characterized by hypopigmented and hyperpigmented macules involving the entire body surface.
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| in_subset | ||
| label |
Dyschromatosis Universalis Hereditaria
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|
| Preferred_Name |
Dyschromatosis Universalis Hereditaria
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| prefixIRI |
NCIT:C173131
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| prefLabel |
Dyschromatosis Universalis Hereditaria
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| Semantic_Type |
Disease or Syndrome
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| UMLS_CUI |
C2930995
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| subClassOf |
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