| Preferred Name |
Skin Hypopigmentation |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C78610 |
| ALT_DEFINITION |
A disorder characterized by loss of skin pigment. A condition characterized by an abnormal loss of color to the skin due to the depletion of melanocytes or melanin. |
| code |
C78610 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118466 |
| Contributing_Source |
NICHD MedDRA |
| DEFINITION |
Abnormal lightening of skin due to decreased melanin production or deposition. Vitiligo, albinism, and leukoderma are among the disorders that are associated with skin hypopigmentation. |
| FULL_SYN |
Hypopigmentation Pigment Dilution |
| Has_NICHD_Parent | |
| label |
Skin Hypopigmentation |
| Legacy_Concept_Name |
Skin_Hypopigmentation |
| NICHD_Hierarchy_Term |
Hypopigmentation |
| Preferred_Name |
Skin Hypopigmentation |
| prefixIRI |
C78610 |
| prefLabel |
Skin Hypopigmentation |
| Semantic_Type |
Finding |
| UMLS_CUI |
C0162835 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/MTHU003037 | Online Mendelian Inheritance in Man | LOOM |