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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:keratoderma hereditarium mutilans
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Accession:EFO:MONDO:0007422 term browser browse the term
Synonyms:exact_synonym: DOID:0111339;   Orphanet:494;   PPK mutilans and deafness;   Vohwinkel syndrome;   http://identifiers.org/medgen/78579;   http://identifiers.org/mesh/C536457;   http://identifiers.org/snomedct/24559001;   http://linkedlifedata.com/resource/umls/id/C0265964;   https://omim.org/entry/124500;   mutilating keratoderma of Vohwinkel;   mutilating keratoderma plus deafness
 related_synonym: KHM;   VOWNKL;   deafness, congenital, with KERATOPACHYDERMIA and constrictions of fingers and toes;   mutilating keratoderma
 alt_id: MONDO:0007422
 xref: DOID:0111339;   GARD:3092;   ICD9:757.39;   MEDGEN:78579;   MESH:C536457;   MIM:124500;   ORDO:494;   SCTID:24559001;   UMLS:C0265964


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            keratoderma hereditarium mutilans 0
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