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orofaciodigital syndrome III

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Human disease

External resources

UMLS CUI
C0406726[1]
GARD rare disease ID
10518[2]
Orphanet ID
2752[1]
DiseasesDB
31980
ICD-10-CM
Q87.0[2]
Mondo ID
MONDO_0009793
ICD-11 (foundation)
1152322841
MeSH descriptor ID
C557817[3]

mapping relation type: përputhje e përpiktë

C557817[1]
Disease Ontology ID
DOID:0060373[1]
OMIM ID
258850[1]

instancë e

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

nënklasë e

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

on focus list of Wikimedia project

WikiProject Medicine

përputhje e saktë

http://purl.obolibrary.org/obo/DOID_0060373[1]
http://identifiers.org/doid/DOID:0060373[5]
http://www.orpha.net/ORDO/Orphanet_2752

Reference

  1. ^ a b c d e f Disease Ontology, 28 gusht 2019, DOID:0060373
  2. ^ a b c d e f Monarch Disease Ontology release 2018-06-29, 28 korrik 2018, MONDO_0009793
  3. ^ Monarch Disease Ontology release 2018-06-29, MONDO_0009793, 28 korrik 2018
  4. ^ Disease Ontology, 15 maj 2019, DOID:0060373
  5. ^ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233
Marrë nga "https://sq.wikipedia.org/wiki/Speciale:AboutTopic/Q7635034"