Disease Browser
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Parent Node: Hearing Loss, Central (D006313) | ..Starting node ..Deafness, autosomal dominant nonsyndromic sensorineural 53 (C538201)
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Sister Nodes: | ..Auditory neuropathy (C538268)
| ..Auditory Neuropathy, Autosomal Dominant, 1 (C563790)
| ..Deafness nephritis ano rectal malformation (C535996)
| ..Deafness, autosomal dominant nonsyndromic sensorineural 3 (C538200)
| ..Deafness, autosomal dominant nonsyndromic sensorineural 53 (C538201)
| ..Deafness, autosomal recessive 51 (C538202)
| ..Deafness, autosomal recessive 55 (C538203)
| ..Deafness, Neural, Congenital Moderate (C565640)
| ..Deafness, neurosensory, autosomal recessive 47 (C538205)
| ..Groll Hirschowitz syndrome (C537305)
| ..Jensen syndrome (C537568)
| ..Mitochondrial myopathy with lactic acidosis (C537476)
| ..Optic atrophy polyneuropathy deafness (C537129)
| ..Ruzicka Goerz Anton syndrome (C537192)
| ..Santos Mateus Leal syndrome (C537235)
| ..Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness (C564769)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 3028 |
Name: | Deafness, autosomal dominant nonsyndromic sensorineural 53 |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D006313 |
TreeNumbers: | C09.218.458.341.887.432/C538201 |C09.218.807.186.432/C538201 |C10.228.140.068.432/C538201 |C10.597.751.418.341.887.432/C538201 |C23.888.592.763.393.341.887.432/C538201 |
Synonyms: | |
Slim Mappings: | Ear-nose-throat disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C538201
MeSH: C538201
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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