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:
expandCarcinoma, Neuroendocrine (D018278)
Parent Node:
expandDental Enamel Hypoplasia (D003744)
Parent Node:
expandHearing Loss, Sensorineural (D006319)
Parent Node:
expandSalivary Gland Neoplasms (D012468)
..Starting node
..expandNeuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia (C566352)

       Child Nodes:



 Sister Nodes: 
..expandNeuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia (C566352)
..expandParotid Neoplasms (D010307) Child1
..expandSalivary Gland Adenoma, Pleomorphic (C563250)
..expandSublingual Gland Neoplasms (D013362)
..expandSubmandibular Gland Neoplasms (D013365)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7952
Name:Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia
Definition:
Alternative IDs:
ParentIDs:MESH:D003744|MESH:D006319|MESH:D012468|MESH:D018278
TreeNumbers:C04.557.465.625.650.240/C566352 |C04.557.470.200.025.370/C566352 |C04.557.580.625.650.240/C566352 |C04.588.443.591.824/C566352 |C07.465.565.824/C566352 |C07.465.815.718/C566352 |C07.650.800.255/C566352 |C07.793.700.255/C566352 |C09.218.458.341.887/C566352 |C10.59
Synonyms:
Slim Mappings:Cancer|Congenital abnormality|Ear-nose-throat disease|Mouth disease|Nervous system disease|Signs and symptoms
Reference: MedGen: C566352
MeSH: C566352
OMIM: 603641;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0000705Amelogenesis imperfecta
3 HP:0006297Enamel hypoplasia
4 HP:0000407Sensorineural hearing impairment
5 HP:0009590Unilateral vestibular Schwannoma
Disease Causing ClinVar Variants