Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Domain and all descendants
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Dysgeusia A condition characterized by alterations of the sense of taste which may range from mild to severe, including gross distortions of taste quality. | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100564 |
| Dyskeratosis Congenita A predominantly X-linked recessive syndrome characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membran… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150099 |
| Dyskinesia, Drug-Induced Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of th… | Toxic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100311 |
| Dyskinesias Abnormal involuntary movements which primarily affect the extremities, trunk, or jaw that occur as a manifestation of an underlying disease process. … | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100308 |
| Dyslexia, Acquired A receptive visual aphasia characterized by the loss of a previously possessed ability to comprehend the meaning or significance of handwritten words… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100458 |
| Dyslipidemias Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL… | Metabolic Disorder | Pathology | Endocrine System [curated_secondary] | AMW:DIS:180039 |
| Dysmenorrhea Painful menstruation. | Pathologic Condition | Pathology | Reproductive System [curated_secondary] | AMW:DIS:230179 |
| Dysostoses Defective bone formation involving individual bones, singly or in combination. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050015 |
| Dyspareunia Recurrent genital pain occurring during, before, or after SEXUAL INTERCOURSE in either the male or the female. | Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120017 |
| Dyspepsia Impaired digestion, especially after eating. | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230299 |
| Dysphagia Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Symptom | Clinical Medicine | Respiratory System [role_derived] | AMW:SYM:145016 |
| Dysphonia Difficulty and/or pain in PHONATION or speaking. | Pathologic Condition | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080035 |
| Dyspnea Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Symptom | Clinical Medicine | Respiratory System [role_derived] | AMW:SYM:135006 |
| Dyssomnias A broad category of sleep disorders characterized by either hypersomnolence or insomnia. The three major subcategories include intrinsic (i.e., arisi… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100631 |
| Dystocia Slow or difficult OBSTETRIC LABOR or CHILDBIRTH. | Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120230 |
| Dystonia An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial … | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100439 |
| Dystonia Musculorum Deformans A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. … | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100057 |
| Dystonic Disorders Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100313 |
| Dysuria Canonical symptom replacement for semantically misclassified source AMW:DIS:230335. | Symptom | Clinical Medicine | Renal and Urinary System [curated_secondary] | AMW:SYM:155010 |
| Ebstein Anomaly A congenital heart defect characterized by downward or apical displacement of the TRICUSPID VALVE, usually with the septal and posterior leaflets bei… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140017 |
| Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | Pathologic Condition | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150064 |
| Echogenic Bowel A PRENATAL ULTRASONOGRAPHY finding of excessively dense fetal bowel due to MECONIUM buildup. | Congenital Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120210 |
| Echolalia Involuntary (parrot-like), meaningless repetition of a recently heard word, phrase, or song. This condition may be associated with transcortical APHA… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100469 |
| Eclampsia Onset of HYPERREFLEXIA; SEIZURES; or COMA in a previously diagnosed pre-eclamptic patient (PRE-ECLAMPSIA). | Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120219 |
| Ectodermal Dysplasia A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnor… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160009 |
| Ectodermal Dysplasia 1, Anhidrotic An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN. | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160010 |
| Ectodermal Dysplasia 3, Anhidrotic An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR. | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160011 |
| Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive An autosomal recessive form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR or EDAR-ASSOCIATED DEATH DOMAIN PROTE… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160012 |
| Ectopia Cordis A rare developmental defect in which the heart is abnormally located partially or totally outside the THORAX. It is the result of defective fusion of… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140018 |
| Ectopia Lentis Congenital displacement of the lens resulting from defective zonule formation. | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110034 |