All terms in DOID

Label Id Description
airborne transmission TRANS_0000009 [Airborne transmission is an indirect transmission process during which the pathogen is indirectly transferred from a reservoir, source or host to another host while suspended in the air as dust.]
Orthoparamyxovirinae NCBITaxon_2560076
cauda equina UBERON_0012337
multi cell part structure UBERON_0005162
multisystem proteinopathy DOID_070355 [A motor neuron disease that has_material_basis_in some inheritance and affects muscle, bone, and the nervous system.]
motor neuron disease DOID_231 [A neurodegenerative disease that is located_in the motor neurons.]
chromosome 17p13.3 duplication syndrome DOID_0060432 [A chromosomal duplication syndrome that has_material_basis_in the PAFAH1B1 and/or the YWHAE gene on chromosome 17p13.3.]
chromosome 17q12 duplication syndrome DOID_0060433 [A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 17q12 region.]
chromosome 17q21.31 duplication syndrome DOID_0060434 [A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 17q21.31 region.]
chromosome 1q21.1 duplication syndrome DOID_0060435 [A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 1q21.1 region.]
chromosome 22q11.2 microduplication syndrome DOID_0060436 [A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 22q11.2 region.]
chromosome 22q13 duplication syndrome DOID_0060437 [A chromosomal duplication syndrome that has_material_basis_in heterozygous interstitial duplication in chromosome 22q13 involving the SHANK3 gene.]
Cole-Carpenter syndrome DOID_0060438 [An osteogenesis imperfecta characterized by craniosynostosis, communicating hydrocephalus, ocular proptosis, marked postnatal growth failure, and distinctive facial appearance.]
osteogenesis imperfecta DOID_12347 [An osteochondrodysplasia that has_material_basis_in a deficiency in type-I collagen which results_in brittle bones and defective connective tissue.]
lysinuric protein intolerance DOID_0060439 [An amino acid metabolic disorder characterized by the body's inability to effectively break down lysine, arginine and ornithine and by renal hyperdiaminoaciduria, especially lysinuria, and by impaired formation of urea with hyperammonemia after protein ingestion. It has_material_basis_in homozygous or compound heterozygous mutation in the amino acid transporter gene SLC7A7 on chromosome 14q11.]
amino acid metabolic disorder DOID_9252 [An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids.]
mandible UBERON_0001684
intramembranous bone UBERON_0002514
dentary UBERON_0004742
Alternaria NCBITaxon_5598