Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| calbc:hasCorrelation | |
| skos:exactMatch | |
| skos:definition |
MSH: An autosomal dominant disorder that is manifested by thickened spongiform ORAL MUCOSA with a white opalescent tint. Other MUCOSAL TISSUE may also be involved mucosa found in the VAGINA; RECTUM, and NASAL CAVITY may be similarly involved. This form of LEUKOKERATOSIS can be caused by a mutation in the gene for KERATIN 4 and is not considered a PRENEOPLASTIC CONDITION.,NCI: An autosomal dominant inherited disorder characterized by thickened and spongy oral mucosa with a white tint. It may affect other anatomic sites as well.
|
| skos:inScheme | |
| skos-xl:prefLabel | |
| skos-xl:altLabel |
umls-label:A10908140,
umls-label:A18435438,
umls-label:A11946643,
umls-label:A10907041,
umls-label:A10908137,
umls-label:A10908757,
umls-label:A17686397,
umls-label:A18442603,
umls-label:A10907042,
umls-label:A10908758,
umls-label:A8355392,
umls-label:A19284624,
umls-label:A18648237,
umls-label:A18442604,
umls-label:A10911946,
umls-label:A19291302,
umls-label:A19293038,
umls-label:A18440189
|