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 |
|---|---|---|---|---|
| Eunuchism The state of being a eunuch, a male without TESTES or whose testes failed to develop. It is characterized by the lack of mature male GERM CELLS and T… | Metabolic Disorder | Pathology | Endocrine System [curated_secondary] | AMW:DIS:190017 |
| Euthyroid Sick Syndromes Conditions of abnormal THYROID HORMONES release in patients with apparently normal THYROID GLAND during severe systemic illness, physical TRAUMA, and… | Syndrome | Pathology | Endocrine System [curated_secondary] | AMW:DIS:190027 |
| Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they wer… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170068 |
| Exercise Intolerance 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:185020 |
| exercise stress test Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Investigation | Investigation | Respiratory System [role_derived] | AMW:TECH:140004 |
| Exercise-Induced Allergies Allergic reactions following a period of exercise. Elevated serum HISTAMINE and TRYPTASE levels and cutaneous MAST CELL degranulation are often assoc… | Immune Disorder | Pathology | Immune System [curated_secondary] | AMW:DIS:200015 |
| Exertional Chest Tightness 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:105040 |
| Exertional 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:135002 |
| Exfoliation Syndrome The deposition of flaky, translucent fibrillar material most conspicuous on the anterior lens capsule and pupillary margin but also in both surfaces … | Syndrome | Pathology | Visual System [curated_secondary] | AMW:DIS:110147 |
| Exocrine Pancreatic Insufficiency A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE)… | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060222 |
| Exophthalmos Abnormal protrusion of both eyes; may be caused by endocrine gland malfunction, malignancy, injury, or paralysis of the extrinsic muscles of the eye. | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110095 |
| Exostoses Benign hypertrophy that projects outward from the surface of bone, often containing a cartilaginous component. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050097 |
| Exotropia A form of ocular misalignment where the visual axes diverge inappropriately. For example, medial rectus muscle weakness may produce this condition as… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100360 |
| Eye Abnormalities Congenital absence of or defects in structures of the eye; may also be hereditary. | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110026 |
| Eye Burns Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation. | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100657 |
| Eye Diseases Diseases affecting the eye. | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110001 |
| Eye Diseases, Hereditary Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the ey… | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110040 |
| Eye Foreign Bodies Inanimate objects that become enclosed in the eye. | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100659 |
| Eye Hemorrhage Intraocular hemorrhage from the vessels of various tissues of the eye. | Vascular Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110055 |
| Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100654 |
| Eye Injuries, Penetrating Deeply perforating or puncturing type intraocular injuries. | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100660 |
| Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | Pathologic Condition | Pathology | Visual System [curated_secondary] | AMW:DIS:110062 |
| Eyelid Diseases Diseases involving the EYELIDS. | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110065 |
| Fabry Disease An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100097 |
| Facial Dermatoses Skin diseases involving the FACE. | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170069 |
| Facial Injuries General or unspecified injuries to the soft tissue or bony portions of the face. | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100653 |
| Factor V Deficiency A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency kn… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150046 |
| Factor VII Deficiency An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependen… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150047 |
| Factor X Deficiency Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150048 |
| Factor XI Deficiency A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting i… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150049 |