લખાણ પર જાઓ

orofaciodigital syndrome III

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લેખ બનાવો

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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 ID (Foundation)
1152322841
MeSH descriptor ID
C557817[૩]

mapping relation type: exact match

C557817[૧]
Disease Ontology ID
DOID:0060373[૧]
OMIM ID
258850[૧]

ઉદાહરણ

head and neck disease[૨]
developmental defect during embryogenesis[૨]
class of disease

નો પેટા-પ્રકાર

oral-facial-digital syndrome[૪]
genetic syndromic intellectual disability[૨]
syndromic genetic deafness[૨]

on focus list of Wikimedia project

WikiProject Medicine

exact match

http://purl.obolibrary.org/obo/DOID_0060373[૧]
http://identifiers.org/doid/DOID:0060373[૫]
http://www.orpha.net/ORDO/Orphanet_2752

સંદર્ભ

  1. ↑ ૧.૦ ૧.૧ ૧.૨ ૧.૩ ૧.૪ ૧.૫ Disease Ontology, ૨૮ ઓગસ્ટ 2019, DOID:0060373
  2. ↑ ૨.૦ ૨.૧ ૨.૨ ૨.૩ ૨.૪ ૨.૫ Monarch Disease Ontology release 2018-06-29, ૨૮ જુલાઇ 2018, MONDO_0009793
  3. ↑ Monarch Disease Ontology release 2018-06-29, MONDO_0009793, ૨૮ જુલાઇ 2018
  4. ↑ Disease Ontology, ૧૫ મે 2019, DOID:0060373
  5. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233
"https://gu.wikipedia.org/wiki/વિશેષ:AboutTopic/Q7635034" થી મેળવેલ