orofaciodigital syndrome III

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Human disease

Risorse esterne

UMLS CUI	C0406726^[1]
identificativo GARD di una malattia rara	10518^[2]
identificativo Orphanet	2752^[1]
identificativo DiseasesDB	31980
ICD-10-CM	Q87.0^[2]
identificativo MonDO	MONDO_0009793
ICD-11 (foundation)	1152322841
identificativo MeSH	C557817^[3] tipo di relazione: corrispondenza esatta C557817^[1]
identificativo Disease Ontology	DOID:0060373^[1]
identificativo OMIM	258850^[1]

head and neck disease^[2]

difetto dello sviluppo durante l'embriogenesi^[2]

classe di malattia

oral-facial-digital syndrome^[4]

genetic syndromic intellectual disability^[2]

syndromic genetic deafness^[2]

Progetto:Medicina

↑ ^1,0 ^1,1 ^1,2 ^1,3 ^1,4 ^1,5 Disease Ontology, 28 Aùs 2019, DOID:0060373
↑ ^2,0 ^2,1 ^2,2 ^2,3 ^2,4 ^2,5 Monarch Disease Ontology release 2018-06-29, 28 lug 2018, MONDO_0009793
↑ Monarch Disease Ontology release 2018-06-29, MONDO_0009793, 28 lug 2018
↑ Disease Ontology, 15 Maj 2019, DOID:0060373
↑ registro identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233