Mine sisu juurde

orofaciodigital syndrome III

Lehekülje sisu ei toetata teistes keeltes.

Human disease

Välised allikad

UMLS CUI
GARD rare disease ID
Orphanet ID
DiseasesDB
ICD-10-CM
Mondo ID
ICD-11 (foundation)
MeSH descriptor ID
C557817[3]

mapping relation type: täpne vaste

Disease Ontology ID
OMIM ID

üksikjuht nähtusest

head and neck disease[2]
developmental defect during embryogenesis[2]
class of disease

mille alamklass

oral-facial-digital syndrome[4]
genetic syndromic intellectual disability[2]
syndromic genetic deafness[2]

Wikimedia projekti fookusnimekiri

Viited

  1. 1,0 1,1 1,2 1,3 1,4 1,5 Disease Ontology, 28. august 2019, DOID:0060373
  2. 2,0 2,1 2,2 2,3 2,4 2,5 Monarch Disease Ontology release 2018-06-29, 28. juuli 2018, MONDO_0009793
  3. Monarch Disease Ontology release 2018-06-29, MONDO_0009793, 28. juuli 2018
  4. Disease Ontology, 15. mai 2019, DOID:0060373
  5. Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233