About: hereditary sensory neuropathy

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Xref MGI. OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	neuropathy
label	hereditary sensory neuropathy
comment	Xref MGI. OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0050548
database_cross_reference	MESH:D009477 OMIM:PS162400
has_exact_synonym	familial dysautonomia, type II (en) hereditary sensory and autonomic neuropathy (en)
has_obo_namespace	disease_ontology
in_subset	DO_FlyBase_slim
http://purl.obolib...g/obo/IAO_0000115	A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.
is subClassOf of	Riley-Day syndrome hereditary sensory and autonomic neuropathy type 5 hereditary sensory neuropathy type 4 hereditary sensory neuropathy type 1B hereditary sensory and autonomic neuropathy type 7 hereditary sensory and autonomic neuropathy type 6 hereditary sensory and autonomic neuropathy type 8 hereditary sensory neuropathy type 1E hereditary sensory neuropathy X-linked atypical hereditary sensory neuropathy hereditary sensory and autonomic neuropathy type 2 hereditary sensory and autonomic neuropathy type 1
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50937096

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