orofaciodigital syndrome III

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Human disease

બાહ્ય સ્રોતો

UMLS CUI	C0406726^[૧]
GARD rare disease ID	10518^[૨]
Orphanet ID	2752^[૧]
DiseasesDB	31980
ICD-10-CM	Q87.0^[૨]
Mondo ID	MONDO_0009793
ICD-11 (foundation)	1152322841
MeSH descriptor ID	C557817^[૩] mapping relation type: exact match C557817^[૧]
Disease Ontology ID	DOID:0060373^[૧]
OMIM ID	258850^[૧]

head and neck disease^[૨]

developmental defect during embryogenesis^[૨]

class of disease

oral-facial-digital syndrome^[૪]

genetic syndromic intellectual disability^[૨]

syndromic genetic deafness^[૨]

WikiProject Medicine

↑ ^૧.૦ ^૧.૧ ^૧.૨ ^૧.૩ ^૧.૪ ^૧.૫ Disease Ontology, ૨૮ ઓગસ્ટ 2019, DOID:0060373
↑ ^૨.૦ ^૨.૧ ^૨.૨ ^૨.૩ ^૨.૪ ^૨.૫ Monarch Disease Ontology release 2018-06-29, ૨૮ જુલાઇ 2018, MONDO_0009793
↑ Monarch Disease Ontology release 2018-06-29, MONDO_0009793, ૨૮ જુલાઇ 2018
↑ Disease Ontology, ૧૫ મે 2019, DOID:0060373
↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233