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