All terms in DOID
| Label | Id | Description |
|---|---|---|
| agraphia | DOID_0060223 | [An acquired writing disorder causing a loss in the ability to communicate through writing, either due to some motor dysfunction or the inability to spell.] |
| VJ_C_cluster | SO_0000489 | [Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one VJ-gene and one C-gene.] |
| VDJ_J_cluster | SO_0000488 | [Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one VDJ-gene and one J-gene.] |
| VDJ_J_C_cluster | SO_0000487 | [Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one VDJ-gene, one J-gene and one C-gene.] |
| five_prime_D_nonamer | SO_0000497 | [9 nucleotide recombination site (e.g. GGTTTTTGT), part of a five_prime_D-recombination signal sequence (SO:0000556) of an immunoglobulin/T-cell receptor gene.] |
| olfactory nerve disease | DOID_367 | [A brain disease that is characterized by nerve injury located_in olfactory nerve, occurring as a result of normal aging, trauma, mass lesion or other insult, and has_symptom impaired sense of smell, has_symptom anosmia or loss of smell.] |
| five_prime_D_heptamer | SO_0000496 | [7 nucleotide recombination site (e.g. CACTGTG), part of a 5' D-recombination signal sequence (SO:0000556) of an immunoglobulin/T-cell receptor gene.] |
| three_prime_D_spacer | SO_0000495 | [A 12 or 23 nucleotide spacer between the 3'D-HEPTAMER and 3'D-NONAMER of a 3'D-RS.] |
| three_prime_D_nonamer | SO_0000494 | [A 9 nucleotide recombination site (e.g. ACAAAAACC), part of a 3' D-recombination signal sequence of an immunoglobulin/T-cell receptor gene.] |
| obsolete spontaneous rupture of bladder | DOID_364 | |
| three_prime_D_heptamer | SO_0000493 | [7 nucleotide recombination site like CACAGTG, part of a 3' D-recombination signal sequence of an immunoglobulin/T-cell receptor gene.] |
| VJ_J_cluster | SO_0000491 | [Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one VJ-gene and one J-gene.] |
| VJ_J_C_cluster | SO_0000490 | [Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one VJ-gene, one J-gene and one C-gene.] |
| Scheie syndrome | DOID_0060222 | [A mucopolysaccharidosis characterized by corneal clouding, facial dysmorphism and normal lifespan.] |
| Maffucci syndrome | DOID_0060221 | [A syndrome characterized by the presence of multiple enchondromas (benign growths of cartilage) associated with multiple hemangiomas.] |
| American histoplasmosis | DOID_1759 | [A histoplasmosis that results in systemic fungal infection, has_material_basis_in Histoplasma capsulatum var capsulatum, transmitted by airborne spores and has symptom nonproductive cough, has symptom headache, has symptom loss of appetite and has symptom muscle pains.] |
| obsolete Histoplasma capsulatum pneumonia | DOID_1758 | [An American histoplasmosis that results_in inflammation located_in lung, has_material_basis_in Histoplasma capsulatum var capsulatum, transmitted_by airborne spores and has_symptom mediastinal lymphadenopathy, has_symptom cough and has_symptom chest pain.] |
| facial hemiatrophy | DOID_1757 | |
| cervix endometriosis | DOID_361 | [A cervix disease that is characterized by the growth endometrial tissue that is located on the cervix.] |
| renal-hepatic-pancreatic dysplasia | DOID_0060259 | [A physical disorder characterized by pancreatic fibrosis, renal dysplasia and hepatic dysgenesis; it is usual fatal soon after birth.] |