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human disease

AttributesValues
rdf:type
owl:sameAs
description
  • human disease (en)
  • մարդու հիվանդություն (hy)
  • хвороба людини (uk)
exact match
exact match
Mondo ID
Mondo ID
Mondo ID
  • MONDO_0008755
rdfs:label
  • Moynahan syndrome (en)
  • syndrome de Moynahan (fr)
skos:prefLabel
  • Moynahan syndrome (en)
  • syndrome de Moynahan (fr)
name
  • Moynahan syndrome (en)
  • syndrome de Moynahan (fr)
instance of
instance of
subclass of
subclass of
Orphanet ID
ICD-10-CM
GARD rare disease ID
OMIM ID
Orphanet ID
  • 2574
ICD-10-CM
  • G40.4
GARD rare disease ID
  • 606
OMIM ID
  • 203600
skos:altLabel
  • Alopecia-epilepsy-intellectual disability syndrome, Moynahan type (en)
  • Moynahan Alopecia Syndrome (en)
  • ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN (en)
UMLS CUI
MeSH descriptor ID
MeSH descriptor ID
UMLS CUI
  • C0265328
MeSH descriptor ID
  • C537052
is owl:sameAs of
is about of
is main subject of
is main subject of
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