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Cell Culture Ontology
Last uploaded:
July 23, 2014
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| Preferred Name | trichorhinophalangeal syndrome type I or III | |
| Synonyms |
trichorhinophalangeal syndrome type 1 and 3 |
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| Definitions |
Trichorhinophalangeal syndrome type I and III are extremely rare inherited multisystem disorders. Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also. |
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| ID |
http://www.ebi.ac.uk/efo/EFO_0700103 |
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| comment |
Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also.
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| database_cross_reference |
Orphanet:77258 UMLS:CN205736
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|
| definition |
Trichorhinophalangeal syndrome type I and III are extremely rare inherited multisystem disorders.
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|
| has_exact_synonym |
trichorhinophalangeal syndrome type 1 and 3
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|
| label |
trichorhinophalangeal syndrome type I or III
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| preferred label |
trichorhinophalangeal syndrome type I or III
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| prefixIRI |
efo:EFO_0700103
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| prefLabel |
trichorhinophalangeal syndrome type I or III
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| subClassOf |
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|---|---|---|---|---|
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| Mapping To | Ontology | Source |
|---|---|---|
| http://www.ebi.ac.uk/efo/EFO_0700103 | EFO | SAME_URI |
| http://www.ebi.ac.uk/efo/EFO_0700103 | EFO | LOOM |
| http://purl.obolibrary.org/obo/MONDO_0019176 | DOVES | LOOM |