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Regulation of Gene Expression Ontolology
Last uploaded:
December 16, 2015
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| Preferred Name | Piebald trait | |
| Synonyms |
PBT |
|
| Definitions |
(PBT) - Autosomal dominant genetic developmental abnormality of pigmentation characterized by congenital patches of white skin and hair that lack melanocytes. |
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| ID |
http://identifiers.org/omim/172800 |
|
| altLabel |
PBT
|
|
| definition |
(PBT) - Autosomal dominant genetic developmental abnormality of pigmentation characterized by congenital patches of white skin and hair that lack melanocytes.
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|
| id |
OMIM:172800
|
|
| notation |
OMIM:172800
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|
| prefLabel |
Piebald trait
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| subClassOf |
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|---|---|---|---|---|
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Create mapping
| Mapping To | Ontology | Source |
|---|---|---|
| http://identifiers.org/omim/172800 | GEXO | SAME_URI |
| http://identifiers.org/omim/172800 | RETO | SAME_URI |
| rgo:34601 | GAMUTS | LOOM |
| http://purl.obolibrary.org/obo/OMIM_172800 | CCO | LOOM |
| http://purl.bioontology.org/ontology/OMIM/172800 | OMIM | LOOM |
| http://identifiers.org/omim/172800 | GEXO | LOOM |
| http://identifiers.org/omim/172800 | RETO | LOOM |