Term info
- UMLS:C0027889 (Orphanet:140471/e)
- MESH:D009477 (Orphanet:140471/e)
- Orphanet:140471 (MONDO:equivalentTo)
- ICD9:356.2 (MONDO:i2s)
- GARD:0012688 (MONDO:equivalentTo)
- DOID:0050548 (MONDO:equivalentTo)
- SCTID:11442006 (MONDO:equivalentTo)
- NCIT:C125386 (MONDO:equivalentTo)
- OMIMPS:162400 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
https://github.com/NCI-Thesaurus/thesaurus-obo-edition/issues/25
An instance of sensory peripheral neuropathy that is caused by an inherited modification of the individual's genome.
http://purl.obolibrary.org/obo/DOID_0050548, http://purl.obolibrary.org/obo/Orphanet_140471, http://linkedlifedata.com/resource/umls/id/C0027889, http://identifiers.org/mesh/D009477, http://purl.obolibrary.org/obo/NCIT_C125386, https://omim.org/phenotypicSeries/PS162400, http://identifiers.org/snomedct/11442006
familial dysautonomia, type II
congenital pain insensitivity, indifference to pain, Congenital, autosomal recessive, hereditary sensory peripheral neuropathy, HSAN, congenital insensitivity to pain, CIP, hereditary sensory neuropathy, hereditary sensory and autonomic neuropathy
hereditary sensory autonomic neuropathy
MONDO:0015364