Public registry
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Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Any direct membership
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Muscular Dystrophy, Duchenne An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcole… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050269 |
| Muscular Dystrophy, Emery-Dreifuss A heterogenous group of inherited muscular dystrophy without the involvement of nervous system. The disease is characterized by MUSCULAR ATROPHY; MUS… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050270 |
| Muscular Dystrophy, Facioscapulohumeral An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder gi… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050273 |
| Muscular Dystrophy, Oculopharyngeal An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutat… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050274 |
| Musculoskeletal Abnormalities Congenital structural abnormalities and deformities of the musculoskeletal system. | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050305 |
| Musculoskeletal Chest Pain Musculoskeletal chest pain used as a ClinicalGraph target concept for pathology / differential. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050335 |
| Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050001 |
| Myalgia Painful sensation in the muscles. | Pathologic Condition | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050277 |
| Myofascial Pain Syndromes Muscular pain in numerous body regions that can be reproduced by pressure on TRIGGER POINTS, localized hardenings in skeletal muscle tissue. Pain is … | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050278 |
| Myoglobinuria The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050296 |
| Myopathies, Nemaline A group of inherited congenital myopathic conditions characterized clinically by weakness, hypotonia, and prominent hypoplasia of proximal muscles in… | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050280 |
| Myopathies, Structural, Congenital A heterogeneous group of diseases characterized by the early onset of hypotonia, developmental delay of motor skills, non-progressive weakness. Each … | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050279 |
| Myopathy, Central Core An inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development. Muscle biopsy reveals a… | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050281 |
| Myositis Inflammation of a muscle or muscle tissue. | Inflammatory Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050282 |
| Myositis Ossificans A disease characterized by bony deposits or the ossification of muscle tissue. | Inflammatory Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050284 |
| Myositis, Inclusion Body Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The spo… | Inflammatory Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050283 |
| Myotonia Congenita Inherited myotonic disorders with early childhood onset MYOTONIA. Muscular hypertrophy is common and myotonia may impair ambulation and other movemen… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050289 |
| Myotonic Disorders Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) … | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050288 |
| Myotonic Dystrophy Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may a… | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050275 |
| Myotoxicity Damage to the muscle or its function secondary to toxic substances such as drugs used in CHEMOTHERAPY; IMMUNOTHERAPY; or RADIATION. | Toxic Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050290 |
| Nail-Patella Syndrome A syndrome of multiple abnormalities characterized by the absence or hypoplasia of the PATELLA and congenital nail dystrophy. It is a genetically det… | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050238 |
| Non-Radiographic Axial Spondyloarthritis Chronic inflammatory conditions affecting the axial joints which cannot be detectable on x-rays. It is characterized by pain, stiffness of joints and… | Inflammatory Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050131 |
| Noonan Syndrome A genetically heterogeneous, multifaceted disorder characterized by short stature, webbed neck, ptosis, skeletal malformations, hypertelorism, hormon… | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050321 |
| Ochronosis The yellowish discoloration of connective tissue due to deposition of HOMOGENTISIC ACID (a brown-black pigment). This is due to defects in the metabo… | Pathologic Condition | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:230193 |
| Ophthalmoplegia, Chronic Progressive External A mitochondrial myopathy characterized by slowly progressive paralysis of the levator palpebrae, orbicularis oculi, and extraocular muscles. Ragged-r… | Metabolic Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050256 |
| Orbital Myositis Inflammation of the extraocular muscle of the eye. It is characterized by swelling which can lead to ischemia, fibrosis, or ORBITAL PSEUDOTUMOR. | Inflammatory Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050285 |
| Orofaciodigital Syndromes Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-li… | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050023 |
| Ossification of Posterior Longitudinal Ligament A calcification of the posterior longitudinal ligament of the spinal column, usually at the level of the cervical spine. It is often associated with … | Pathologic Condition | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050118 |
| Osteitis Inflammation of the bone. | Inflammatory Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050102 |
| Osteitis Deformans A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of… | Inflammatory Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050103 |