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loading...| Preferred Name | Ectrodactyly | |
| Synonyms |
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|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Ectrodactyly |
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| ID |
C75000 |
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| NCI_Definition |
A rare genetic disorder often inherited in an autosomal manner characterized by limb malformations including syndactyly, median clefts of the hands and/or feet, and partial or complete absence of fingers or toes. It may be associated with other skeletal and extraskeletal abnormalities. |
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| NCI_PT |
Split-Hand/Foot Malformation |
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| NICHD_Definition |
_ |
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| prefixIRI |
Ectrodactyly |
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| prefLabel |
Ectrodactyly |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Genetic_Disorder |
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