Other hereditary and idiopathic neuropathies

Preferred Label : Other hereditary and idiopathic neuropathies;

Inclusion CIM-10 : Nelaton's syndrome; Dominantly inherited sensory neuropathy; Recessively inherited sensory neuropathy; Morvan's disease;

Diag associé à un acte (%) : 74.7;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

G608;

UMLS CUI

C0477392;

Automatic exact mappings (from CISMeF team)
- Neuropathy, hereditary sensory and autonomic, type iia [OMIM Phenotype]
- morvan disease [MeSH concept]
- syringomyelia [MeSH Descriptor]
DO Cross reference
- hereditary sensory and autonomic neuropathy type 6 [DO Concept]
- hereditary sensory and autonomic neuropathy type 7 [DO Concept]
- hereditary sensory neuropathy type 1E [DO Concept]
Orphanet concepts
- Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome [ORDO Disease]
- Autosomal dominant hereditary sensory and autonomic neuropathy [ORDO Disease]
- Autosomal recessive hereditary sensory and autonomic neuropathy [ORDO Disease]
- Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome [ORDO Disease]
- Cervical hypertrichosis-peripheral neuropathy syndrome [ORDO Disease]
- Chronic relapsing inflammatory optic neuropathy [ORDO Disease]
- Congenital insensitivity to pain with severe intellectual disability [ORDO Disease]
- Congenital insensitivity to pain-anosmia-neuropathic arthropathy [ORDO Disease]
- Congenital insensitivity to pain-hyperhidrosis-absence of cutaneous sensory innervation [ORDO Disease]
- Deafness-small bowel diverticulosis-neuropathy syndrome [ORDO Disease]
- EMILIN-1-related connective tissue disease [ORDO Disease]
- Giant axonal neuropathy [ORDO Disease]
- Hereditary sensory and autonomic neuropathy [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 1 [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 1B [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 2 [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 4 [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 5 [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 6 [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 7 [ORDO Disease]
- Hereditary sensory and autonomic neuropathy type 8 [ORDO Disease]
- Hereditary sensory and autonomic neuropathy with deafness and global delay [ORDO Disease]
- Hereditary sensory neuropathy-deafness-dementia syndrome [ORDO Disease]
- Hypomyelination neuropathy-arthrogryposis syndrome [ORDO Disease]
- Infantile axonal neuropathy [ORDO Disease]
- Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome [ORDO Disease]
- Morvan syndrome [ORDO Disease]
- Mutilating hereditary sensory neuropathy with spastic paraplegia [ORDO Disease]
- Neuropathy with hearing impairment [ORDO Disease]
- Ocular anomalies-axonal neuropathy-developmental delay syndrome [ORDO Disease]
- Peripheral motor neuropathy-dysautonomia syndrome [ORDO Disease]
- PrP systemic amyloidosis [ORDO Disease]
- X-linked hereditary sensory and autonomic neuropathy with deafness [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Hereditary sensory and autonomic neuropathy type I [ICD-11 Subcategory]
- Hereditary sensory and autonomic neuropathy type V [ICD-11 Subcategory]
- hereditary sensory and autonomic neuropathy type 1 [DO Concept]
- hereditary sensory and autonomic neuropathy type 5 [DO Concept]
- hereditary sensory and autonomic neuropathy type 6 [DO Concept]
- hereditary sensory and autonomic neuropathy type 7 [DO Concept]
- hereditary sensory neuropathy type 1B [DO Concept]
- hereditary sensory neuropathy type 1E [DO Concept]
- hereditary sensory neuropathy type 4 [DO Concept]
Validated automatic mappings to NTBT
- syringomyelia [MeSH Descriptor]

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