DOOR syndrome
human disease
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DOOR syndrome
Summary
DOOR syndrome is a rare disease[1]. It draws 3 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2]
Key Facts
- DOOR syndrome's instance of is recorded as rare disease[3].
- DOOR syndrome's instance of is recorded as class of disease[4].
- DOOR syndrome's subclass of is recorded as syndromic intellectual disability[5].
- DOOR syndrome's subclass of is recorded as deafness-onychodystrophy syndrome[6].
- DOOR syndrome's subclass of is recorded as syndrome[7].
- DOOR syndrome's subclass of is recorded as autosomal recessive disease[8].
- DOOR syndrome's OMIM ID is recorded as 220500[9].
- DOOR syndrome's ICD-10 ID is recorded as Q87.8[10].
- DOOR syndrome's DiseasesDB is recorded as 32494[11].
- DOOR syndrome's KEGG ID is recorded as H02218[12].
- DOOR syndrome's Disease Ontology ID is recorded as DOID:0111627[13].
- DOOR syndrome's Orphanet ID is recorded as 79500[14].
- DOOR syndrome's health specialty is recorded as medical genetics[15].
- DOOR syndrome's genetic association is recorded as TBC1D24[16].
- DOOR syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111627[17].
- DOOR syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111627[18].
- DOOR syndrome's GARD rare disease ID is recorded as 1685[19].
- DOOR syndrome's Mondo ID is recorded as MONDO_0009079[20].
- DOOR syndrome's Microsoft Academic ID is recorded as 2777088204[21].
- DOOR syndrome's ICD-11 ID is recorded as 1781537287[22].
- DOOR syndrome's WikiProjectMed ID is recorded as DOOR syndrome[23].
- DOOR syndrome's UniProt disease ID is recorded as DI-03992[24].
Why It Matters
DOOR syndrome draws 3 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2]