All terms in DOID
| Label | Id | Description |
|---|---|---|
| nose symptom | SYMP_0000388 | |
| obsolete fetal or neonatal hemorrhage | DOID_2027 | |
| hemal spine | UBERON_2001364 | |
| endochondral bone | UBERON_0002513 | |
| bone of dorsum | UBERON_0004247 | |
| obsolete malignant extraskeletal cartilaginous and osseous tumor | DOID_3359 | |
| benign epilepsy with centrotemporal spikes | DOID_3329 | |
| childhood electroclinical syndrome | DOID_0050704 | [An electroclinical syndrome with onset in childhood between one and 12 years of age.] |
| sneezing | SYMP_0000139 | [Sneezing is a respiratory system and chest symptom characterized by a sudden violent spasmodic audible expiration of breath through the nose and mouth especially as a reflex act following irritation of the nasal mucous membrane.] |
| respiratory system and chest symptom | SYMP_0000514 | |
| Zygodontomys brevicauda | NCBITaxon_157541 | |
| Zygodontomys | NCBITaxon_157540 | |
| Abnormality of digestive system morphology | HP_0025033 | [A structural anomaly of the digestive system.] |
| Abnormality of the digestive system | HP_0025031 | |
| direction_attribute | SO_0001029 | |
| feature_attribute | SO_0000733 | [An attribute describing a located_sequence_feature.] |
| diplotype | SO_0001028 | [A diplotype is a pair of haplotypes from a given individual. It is a genotype where the phase is known.] |
| variant_collection | SO_0001507 | [A collection of one or more sequences of an individual.] |
| Phenotypic abnormality | HP_0000118 | [A phenotypic abnormality.] |
| genotype | SO_0001027 | [A genotype is a variant genome, complete or incomplete.] |