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loading...| Preferred Name |
hereditary sensory neuropathy |
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| Synonyms |
hereditary sensory and autonomic neuropathy familial dysautonomia, type II |
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| Definitions |
Xref MGI. OMIM mapping confirmed by DO. [SN]. A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages. |
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| ID |
http://purl.obolibrary.org/obo/DOID_0050548 |
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| comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
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| database_cross_reference |
MESH:D009477 OMIM:PS162400 |
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| definition |
A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages. |
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| has exact synonym |
hereditary sensory and autonomic neuropathy familial dysautonomia, type II |
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| has_obo_namespace |
disease_ontology |
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| id |
DOID:0050548 |
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| in_subset | ||
| label |
hereditary sensory neuropathy |
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| notation |
DOID:0050548 |
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| prefLabel |
hereditary sensory neuropathy |
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| subClassOf |
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