Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHereditary Sensory and Autonomic Neuropathies (D009477)
Parent Node:
expandHypertrichosis (D006983)
..Starting node
..expandCervical hypertrichosis neuropathy (C537956)

       Child Nodes:



 Sister Nodes: 
..expandAcromegaloid facial appearance syndrome (C535655)
..expandAmaurosis hypertrichosis (C536604)
..expandAmbras syndrome (C536605)
..expandBarber Say syndrome (C537908)
..expandCAHMR syndrome (C537959)
..expandCantu syndrome (C535572)
..expandCervical hypertrichosis neuropathy (C537956)
..expandCervical Hypertrichosis with Underlying Kyphoscoliosis (C566142)
..expandCongenital hypertrichosis lanuginosa (C538389)
..expandFacial Hypertrichosis (C565029)
..expandFibromatosis, Gingival, with Hypertrichosis and Mental Retardation (C565331)
..expandGorlin Chaudhry Moss syndrome (C537290)
..expandHairy Ears (C562484)
..expandHairy Ears, Y-Linked (C564029)
..expandHairy elbows (C535618)
..expandHairy nose tip (C535619)
..expandHypertrichosis congenital generalized X-linked (C538388)
..expandHypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia (C565016)
..expandHypertrichosis, anterior cervical (C538390)
..expandHypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy (C565492)
..expandHypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features (C538391)
..expandMidphalangeal hair (C537471)
..expandMuller Barth Menger syndrome (C537370)
..expandOliver-McFarlane syndrome (C536554)
..expandRamon Syndrome (C535285)
..expandSchaap Taylor Baraitser syndrome (C536626)
..expandWiedemann Grosse Dibbern syndrome (C536704)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1986
Name:Cervical hypertrichosis neuropathy
Definition:
Alternative IDs:
ParentIDs:MESH:D006983|MESH:D009477
TreeNumbers:C10.114.750.137/C537956 |C10.314.750.600/C537956 |C10.500.310/C537956 |C10.574.500.496/C537956 |C10.668.829.800.625/C537956 |C10.668.829.800.750.450/C537956 |C16.131.666.310/C537956 |C16.320.400.415/C537956 |C17.800.329.875/C537956 |C20.111.258.750.600/C537956
Synonyms:
Slim Mappings:Congenital abnormality|Genetic disease (inborn)|Immune system disease|Nervous system disease|Skin disease
Reference: MedGen: C537956
MeSH: C537956
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants