All terms in DOID

Label Id Description
Pulicomorpha NCBITaxon_140693
Rhabdoviridae NCBITaxon_11270
Prunus armeniaca NCBITaxon_36596
Prunus NCBITaxon_3754
Tremellomycetes NCBITaxon_155616
Abnormal language feature HP_4000072
human respiratory syncytial virus NCBITaxon_11250
Involuntary vocalization HP_4000074
tubular aggregate myopathy 1 DOID_0080089 [A myopathy that is characterized by the presence of tubular aggregates in myofibrils and has_material_basis_in heterozygous mutation in the STIM1 gene on chromosome 11p15.]
obsolete Rotator cuff shoulder syndrome and allied disorder DOID_12702
hyperprolactinemia DOID_12700 [An acquired metabolic disease that has_material_basis_in the presence of abnormally-high levels of prolactin in the blood.]
Pneumoviridae NCBITaxon_11244
Scylla paramamosain NCBITaxon_85552
nonsyndromic congenital nail disorder 2 DOID_0080080 [A nonsyndromic congenital nail disorder that is characterized by nails that are abnormally thin and concave from side to side, with turned up edges.]
nonsyndromic congenital nail disorder DOID_0080683 [A nail disease that is characterized by underdevelopment of nails.]
myoclonic cerebellar dyssynergia DOID_12707
Friedreich ataxia DOID_12705
ataxia telangiectasia DOID_12704 [An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22.]
nonsyndromic congenital nail disorder 7 DOID_0080085 [A nonsyndromic congenital nail disorder that is characterized by nails with longi- tudinal streaks, thinning of the nail plate, poorly developed or absent lunulae, along with variously disturbed formation of the nail plate leading to increased vulnerability of the free nail margins.]
nonsyndromic congenital nail disorder 8 DOID_0080086 [A nonsyndromic congenital nail disorder that is characterized by dystrophy of the toenails only.]