loading...| Preferred Name |
hereditary sensory neuropathy |
|
| Synonyms |
hereditary sensory and autonomic neuropathy familial dysautonomia, type II |
|
| Definitions |
A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0050548 |
|
| comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| database_cross_reference |
MESH:D009477 OMIM:PS162400 |
|
| definition |
A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| has_exact_synonym |
hereditary sensory and autonomic neuropathy familial dysautonomia, type II |
|
| has_obo_namespace |
disease_ontology |
|
| IAO_0000115 |
A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages. |
|
| id |
DOID:0050548 |
|
| in_subset | ||
| label |
hereditary sensory neuropathy |
|
| notation |
DOID:0050548 |
|
| note |
A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| prefLabel |
hereditary sensory neuropathy |
|
| subClassOf |