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loading...| Preferred Name |
Keratoderma, palmoplantar, with deafness |
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| Synonyms |
PPKDFN |
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| Definitions |
(PPKDFN) - An autosomal dominant disorder characterized by the association of palmoplantar hyperkeratosis with progressive, bilateral, high-frequency, sensorineural deafness. |
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| ID |
http://identifiers.org/omim/148350 |
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| altLabel |
PPKDFN |
|
| definition |
(PPKDFN) - An autosomal dominant disorder characterized by the association of palmoplantar hyperkeratosis with progressive, bilateral, high-frequency, sensorineural deafness. |
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| id |
OMIM:148350 |
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| notation |
OMIM:148350 |
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| prefLabel |
Keratoderma, palmoplantar, with deafness |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://identifiers.org/omim/148350 | GEXO | SAME_URI | |
| http://identifiers.org/omim/148350 | RETO | SAME_URI | |
| http://identifiers.org/omim/148350 | GEXO | LOOM | |
| http://identifiers.org/omim/148350 | RETO | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/148350 | OMIM | LOOM | |
| http://purl.obolibrary.org/obo/OMIM_148350 | CCO | LOOM |