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 |
|---|---|---|---|---|
| Hernia, Abdominal A protrusion of abdominal structures through the retaining ABDOMINAL WALL. It involves two parts: an opening in the abdominal wall, and a hernia sac … | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230017 |
| Hernia, Diaphragmatic Protrusion of abdominal structures into the THORAX as a result of congenital or traumatic defects in the respiratory DIAPHRAGM. | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230024 |
| Hernia, Diaphragmatic, Traumatic The type of DIAPHRAGMATIC HERNIA caused by TRAUMA or injury, usually to the ABDOMEN. | Traumatic Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:230025 |
| Hernia, Femoral A groin hernia occurring inferior to the inguinal ligament and medial to the FEMORAL VEIN and FEMORAL ARTERY. The femoral hernia sac has a small neck… | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230018 |
| Hernia, Hiatal STOMACH herniation located at or near the diaphragmatic opening for the ESOPHAGUS, the esophageal hiatus. | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230026 |
| Hernia, Inguinal An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur t… | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230019 |
| Hernia, Obturator A pelvic hernia through the obturator foramen, a large aperture in the hip bone normally covered by a membrane. Obturator hernia can lead to intestin… | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230021 |
| Hernia, Ventral A hernia caused by weakness of the anterior ABDOMINAL WALL due to midline defects, previous incisions, or increased intra-abdominal pressure. Ventral… | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230020 |
| Heterotaxy Syndrome Abnormal thoracoabdominal VISCERA arrangement (visceral heterotaxy) or malformation that involves additional CONGENITAL HEART DEFECTS (e.g., heart is… | Syndrome | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140029 |
| Hiccup A spasm of the diaphragm that causes a sudden inhalation followed by rapid closure of the glottis which produces a sound. | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230308 |
| Hidradenitis The inflammation of a sweat gland (usually of the apocrine type). The condition can be idiopathic or occur as a result of or in association with anot… | Inflammatory Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170149 |
| High Dietary Salt Intake Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Risk Factor | Clinical Medicine | Respiratory System [role_derived] | AMW:RISK:105008 |
| High Pressure Neurological Syndrome A syndrome related to increased atmospheric pressure and characterized by tremors, nausea, dizziness, decreased motor and mental performance, and SEI… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100303 |
| Hip Contracture Permanent fixation of the hip in primary positions, with limited passive or active motion at the hip joint. Locomotion is difficult and pain is somet… | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050216 |
| Hip Dislocation Displacement of the femur bone from its normal position at the HIP JOINT. | Traumatic Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050231 |
| Hip Dislocation, Congenital Congenital dislocation of the hip generally includes subluxation of the femoral head, acetabular dysplasia, and complete dislocation of the femoral h… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050325 |
| Hippocampal Sclerosis Neuronal loss in the hippocampal regions of CA1 and CA4 and less severely CA2 and CA3. Additional loss of hippocampal stratum radiatum, hippocampal a… | Degenerative Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100391 |
| Hirschsprung Disease Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment… | Congenital Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060035 |
| Hirsutism A condition observed in WOMEN and CHILDREN when there is excess coarse body hair of an adult male distribution pattern, such as facial and chest area… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170075 |
| Histiocytic Necrotizing Lymphadenitis Development of lesions in the lymph node characterized by infiltration of the cortex or paracortex by large collections of proliferating histiocytes … | Inflammatory Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150142 |
| Histiocytosis General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinica… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150135 |
| Histiocytosis, Langerhans-Cell A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characte… | Disorder | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080052 |
| Histiocytosis, Non-Langerhans-Cell Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group i… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150136 |
| Histiocytosis, Sinus Benign, non-Langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosi… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150138 |
| Hoarseness Canonical symptom replacement for semantically misclassified source AMW:DIS:080036. | Symptom | Clinical Medicine | Respiratory System [curated_secondary] | AMW:SYM:115008 |
| Holoprosencephaly Anterior midline brain, cranial, and facial malformations resulting from the failure of the embryonic prosencephalon to undergo segmentation and clea… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050312 |
| Homocystinuria Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevation… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100087 |
| Horner Syndrome A syndrome associated with defective sympathetic innervation to one side of the face, including the eye. Clinical features include MIOSIS; mild BLEPH… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100032 |
| Huntington Disease A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100058 |
| Hyaline Membrane Disease A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized b… | Congenital Disorder | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080089 |