|
peripheral retinal degeneration
|
DOID_12161 |
|
|
retinal lattice degeneration
|
DOID_12165 |
|
|
Blessig's cysts
|
DOID_12164 |
|
|
senile reticular retinal degeneration
|
DOID_12163 |
|
|
pseudoretinitis pigmentosa
|
DOID_12162 |
|
|
active cochlear Meniere's disease
|
DOID_13492 |
|
|
Meniere's disease
|
DOID_9849 |
[A vestibular disease characterized by vertigo, low-pitched tinnitus and hearing loss.] |
|
active vestibular Meniere's disease
|
DOID_13491 |
|
|
active cochleovestibular Meniere's disease
|
DOID_13490 |
|
|
nerve compression syndrome
|
DOID_573 |
|
|
ulnar nerve lesion
|
DOID_12168 |
|
|
mononeuritis of upper limb and mononeuritis multiplex
|
DOID_572 |
|
|
urethral syndrome
|
DOID_13498 |
|
|
secondary vitreoretinal degeneration
|
DOID_12167 |
|
|
dyshormonogenic goiter
|
DOID_12175 |
|
|
radial neuropathy
|
DOID_12171 |
|
|
radial nerve lesion
|
DOID_12170 |
|
|
tinea corporis
|
DOID_12179 |
[A dermatophytosis that results_in fungal infection located_in skin, limited to the stratum corneum of the epidermis, has_material_basis_in Ascomycota fungi that belong to a group called dermatophytes and has_symptom itching, and has_symptom red colored skin rash. The border of the rash lesions look scaly.] |
|
obsolete Fetal Macrosomia
|
DOID_12180 |
|
|
Charcot-Marie-Tooth disease axonal type 2JJ
|
DOID_0051043 |
[A Charcot-Marie-Tooth disease type 2 that is characterized by adult onset of distal sensory impairment and distal muscle weakness and atrophy predominantly affecting the lower limbs and that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26.] |
