Jump to:
loading...| Preferred Name |
Palmoplantar Keratoderma |
|
| Synonyms |
|
|
| Definitions |
A group of autosomal dominant, autosomal recessive, X-linked inherited or acquired disorders characterized by the thickening of the palms and soles due to hyperkeratosis. |
|
| ID |
http://purl.obolibrary.org/obo/NCIT_C34748 |
|
| ALT_DEFINITION |
A group of skin disorders characterized by thickening of the palms and soles due to hyperkeratosis. |
|
| code |
C34748 |
|
| Contributing_Source |
MedDRA NICHD |
|
| definition |
A group of autosomal dominant, autosomal recessive, X-linked inherited or acquired disorders characterized by the thickening of the palms and soles due to hyperkeratosis. |
|
| in_subset | ||
| label |
Palmoplantar Keratoderma |
|
| Legacy Concept Name |
Palmoplantar_Keratoderma |
|
| Maps_To |
Palmoplantar keratoderma |
|
| Preferred_Name |
Palmoplantar Keratoderma |
|
| prefixIRI |
NCIT:C34748 |
|
| prefLabel |
Palmoplantar Keratoderma |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C4229552 |
|
| subClassOf |
Create mapping