ವಿಷಯಕ್ಕೆ ಹೋಗು

orofaciodigital syndrome III

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Human disease

External resources

UMLS CUI
C0406726[೧]
GARD rare disease ID
10518[೨]
Orphanet ID
2752[೧]
DiseasesDB
31980
ICD-10-CM
Q87.0[೨]
Mondo ID
MONDO_0009793
ICD-11 (foundation)
1152322841
MeSH descriptor ID
C557817[೩]

mapping relation type: exact match

C557817[೧]
Disease Ontology ID
DOID:0060373[೧]
OMIM ID
258850[೧]

ಉದಾಹರಣೆಗೆ

head and neck disease[೨]
developmental defect during embryogenesis[೨]
class of disease

ಉಪವರ್ಗ

oral-facial-digital syndrome[೪]
genetic syndromic intellectual disability[೨]
syndromic genetic deafness[೨]

on focus list of Wikimedia project

WikiProject Medicine

exact match

http://purl.obolibrary.org/obo/DOID_0060373[೧]
http://identifiers.org/doid/DOID:0060373[೫]
http://www.orpha.net/ORDO/Orphanet_2752

Reference

  1. ↑ ೧.೦ ೧.೧ ೧.೨ ೧.೩ ೧.೪ ೧.೫ Disease Ontology, ೨೮ ಆಗಸ್ಟ್ 2019, DOID:0060373
  2. ↑ ೨.೦ ೨.೧ ೨.೨ ೨.೩ ೨.೪ ೨.೫ Monarch Disease Ontology release 2018-06-29, ೨೮ ಜುಲೈ 2018, MONDO_0009793
  3. ↑ Monarch Disease Ontology release 2018-06-29, MONDO_0009793, ೨೮ ಜುಲೈ 2018
  4. ↑ Disease Ontology, ೧೫ ಮೇ 2019, DOID:0060373
  5. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233
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