ZFIN Human Disease: hereditary sensory neuropathy type 1B

OBO ID: DOID:0070148

Term Name:	hereditary sensory neuropathy type 1B		Search Ontology:
Synonyms:	hereditary sensory neuropathy type IB HSAN with cough and gastroesophageal reflux
Definition:	A hereditary sensory neuropathy characterized by axonal neuropathy with distal sensory impairment, cough, and gastroesophageal reflux that has_material_basis_in variation in the chromosome region 3p24-p22. (2)
References:	MESH:C564296 OMIM:608088 ORDO:139564 SNOMEDCT_US_2023_03_01:717825008 UMLS_CUI:C1842586
Ontology:	Human Disease ( DOID:0070148 )

Relationships

is a type of:	autosomal dominant disease hereditary sensory neuropathy autosomal dominant disease hereditary sensory neuropathy Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None