Palmoplantar Keratoderma with Deafness

Preferred Label : Palmoplantar Keratoderma with Deafness;

MeSH synonym : palmoplantar keratoderma and sensorineural deafness; focal palmoplantar keratoderma with sensorineural deafness; hereditary palmoplantar keratoderma with deafness; keratoderma palmoplantar, with deafness; diffuse palmoplantar keratoderma with deafness; keratoderma, palmoplantar, with deafness; Ppk-Deafness Syndrome; Palmoplantar Hyperkeratosis-Deafness Syndrome; Palmoplantar Hyperkeratosis-Hearing Loss Syndrome; Palmoplantar Keratoderma-Deafness Syndrome; Palmoplantar Keratoderma-Hearing Loss Syndrome; Ppk with Deafness; Keratoderma palmoplantar deafness;

Details

Origin ID

C536152;

UMLS CUI

C1835672;

Automatic exact mappings (from CISMeF team)
- palmoplantar keratoderma-deafness syndrome [DO Concept]
Currated CISMeF NLP mapping
- Keratoderma, palmoplantar, with deafness [OMIM Phenotype]
- Palmoplantar keratoderma with deafness syndrome (disorder) [SNOMED CT concept]
- Palmoplantar keratoderma-deafness syndrome [ORDO Disease]
DO Cross reference
- palmoplantar keratoderma-deafness syndrome [DO Concept]
Has phenotype(s) (HPO)
- high, narrow forehead [HPO term]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
- keratoderma, palmoplantar [MeSH Descriptor]
ORDO relation(s)
- Palmoplantar keratoderma-deafness syndrome [ORDO Disease]
Record concept(s)
- Palmoplantar Keratoderma with Deafness [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Keratoderma, palmoplantar, with deafness [OMIM Phenotype]
- Palmoplantar keratoderma with deafness syndrome (disorder) [SNOMED CT concept]
- Palmoplantar keratoderma-deafness syndrome [ORDO Disease]
- palmoplantar keratoderma-deafness syndrome [DO Concept]

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