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About:
hypotrichosis
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Xref MGI.
Attributes
Values
type
Class
subClassOf
hair disease
label
hypotrichosis
comment
Xref MGI.
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:4535
database_cross_reference
MESH:D007039
OMIM:PS605389
ORDO:55654
SNOMEDCT_US_2021_09_01:53602002
UMLS_CUI:C0020678
has_obo_namespace
disease_ontology
in_subset
DO_rare_slim
NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115
A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles.
is
subClassOf
of
hypotrichosis of eyelid
hypotrichosis 14
hypotrichosis 1
hypotrichosis 2
hypotrichosis 3
hypotrichosis 4
hypotrichosis 5
hypotrichosis 6
hypotrichosis 7
hypotrichosis 8
hypotrichosis 9
hypotrichosis 10
hypotrichosis 11
hypotrichosis 12
hypotrichosis 13
congenital hypotrichosis with juvenile macular dystrophy
alopecia
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50953087
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