Disease Browser
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Parent Node: Usher Syndromes (D052245) | ..Starting node ..Usher Syndrome, Type ID/F (C567409)
| Child Nodes:
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Sister Nodes: | ..Usher syndrome, type 1B (C536485)
| ..Usher syndrome, type 1C (C536486)
| ..Usher syndrome, type 1D (C536487)
| ..Usher syndrome, type 1E (C536488)
| ..Usher syndrome, type 1F (C536489)
| ..Usher syndrome, type 2A (C536490)
| ..Usher syndrome, type 2B (C536491)
| ..Usher syndrome, type 2C (C536492)
| ..Usher Syndrome, Type Ib (C564755)
| ..Usher Syndrome, Type IC (C564753)
| ..Usher Syndrome, Type ID (C563400)
| ..Usher Syndrome, Type ID/F (C567409)
| ..Usher Syndrome, Type IE (C566577)
| ..Usher Syndrome, Type IF (C566586)
| ..Usher Syndrome, Type IG (C564643)
| ..Usher Syndrome, Type IH (C567227)
| ..USHER SYNDROME, TYPE IID (OMIM:611383)
| ..USHER SYNDROME, TYPE IIIA (OMIM:276902)
| ..USHER SYNDROME, TYPE IJ (OMIM:614869)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 11455 |
Name: | Usher Syndrome, Type ID/F |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D052245 |
TreeNumbers: | C09.218.458.341.186.500.500/C567409 |C09.218.458.341.887.886/C567409 |C10.597.751.418.341.186.500.500/C567409 |C10.597.751.418.341.887.886/C567409 |C10.597.751.941.162.625.500/C567409 |C11.768.585.658.500.813/C567409 |C11.966.075.375.500/C567409 |C16.131.077.29 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Ear-nose-throat disease|Eye disease|Genetic disease (inborn)|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C567409
MeSH: C567409
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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