All terms in DOID

Label Id Description
muscle necrosis SYMP_0000334
soft tissue necrosis SYMP_0020062 [A musculoskeletal system symptom that is characterized by necrosis (i.e. tissue death) of soft tissue, including muscle, fat, blood vessels, nerves, tendons, and tissues that surround the bones and joints.]
neck weakness SYMP_0000335
neck symptom SYMP_0000384
muscle soreness SYMP_0000332
autosomal dominant nonsyndromic deafness 81 DOID_0070608 [An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ELMOD3 gene on chromosome 2p11.]
muscle tenderness SYMP_0000333
autosomal dominant nonsyndromic deafness 83 DOID_0070609 [An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the MAP1B gene on chromosome 5q13.]
obsolete joint derangement DOID_2279
mouth sore SYMP_0000330
autosomal dominant nonsyndromic deafness 87 DOID_0070606 [An autosomal dominant nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss with inner ear anomalies, including cochlear maldevelopment, absence of the osseous spiral lamina, and/or an enlarged vestibular aqueduct that has_material_basis_in heterozygous mutation in the PI4KB gene on chromosome 1q21.]
muscle ache SYMP_0000331 [A pain that is characterized by a continuous or prolonged dull pain.]
muscle pain SYMP_0019161 [A pain that is characterized by a pain in one or more muscles.]
autosomal dominant nonsyndromic deafness 90 DOID_0070607 [An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the MYO3A gene on chromosome 10p12.]
benzylpenicillin CHEBI_18208
autosomal dominant nonsyndromic deafness 84 DOID_0070604 [An autosomal dominant nonsyndromic deafness characterized by bilateral, progressive sensorineural hearing loss with variable onset and audiogram shape that has_material_basis_in heterozygous mutation in the ATP11A gene on chromosome 13q34.]
autosomal dominant nonsyndromic deafness 85 DOID_0070605 [An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the USP48 gene on chromosome 1p36.]
organic hydroxy compound CHEBI_33822
Micrognathia HP_0000347
Aplasia/Hypoplasia of the mandible HP_0009118