orofaciodigital syndrome III

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Human disease

Adnoddau allanol

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
dynodwr MeSH	C557817^[3] mapping relation type: exact match C557817^[1]
Disease Ontology ID	DOID:0060373^[1]
dynodwr OMIM	258850^[1]

clwyf y pen a'r ysgwyddau^[2]

developmental defect during embryogenesis^[2]

dosbarth o glefyd

oral-facial-digital syndrome^[4]

genetic syndromic intellectual disability^[2]

syndromic genetic deafness^[2]

↑ ^1.0 ^1.1 ^1.2 ^1.3 ^1.4 ^1.5 Disease Ontology, 28 Awst 2019, DOID:0060373
↑ ^2.0 ^2.1 ^2.2 ^2.3 ^2.4 ^2.5 Monarch Disease Ontology release 2018-06-29, 28 Gorffennaf 2018, MONDO_0009793
↑ Monarch Disease Ontology release 2018-06-29, MONDO_0009793, 28 Gorffennaf 2018
↑ Disease Ontology, 15 Mai 2019, DOID:0060373
↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233