Link to this page
Regulation of Transcription Ontology
Last uploaded:
December 4, 2018
Jump to:
| Id | http://identifiers.org/omim/172800
http://identifiers.org/omim/172800
|
|---|---|
| Preferred Name | Piebald trait |
| Definitions |
(PBT) - Autosomal dominant genetic developmental abnormality of pigmentation characterized by congenital patches of white skin and hair that lack melanocytes.
|
| Synonyms |
PBT
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | (PBT) - Autosomal dominant genetic developmental abnormality of pigmentation characterized by congenital patches of white skin and hair that lack melanocytes. |
|---|---|
| altLabel |
PBT
|
| prefLabel |
Piebald trait
|
| notation |
OMIM:172800
|
| id |
OMIM:172800
|
| subClassOf | |
| type |
Add comment
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |