rhabdoid tumor
childhood kidney neoplasm that is located in the in the kidney as well as other locations outside the kidneys such as the liver, muscle, heart, lung, soft tissues, skin, the central nervous system
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Summary
rhabdoid tumor is a class of disease[1]. It draws 144 Wikipedia views per month (class of disease category, ranking #626 of 1,968).[2]
Key Facts
- Subclass of: childhood kidney neoplasm[3]
- Commons category: Malignant rhabdoid tumors[4]
- NCI Thesaurus ID: C3808[5]
- Health specialty: oncology[6]
- Genetic association: SMARCA4[7], SMARCB1[8]
- Age of onset: congenital onset[9], childhood onset[10], infantile onset[11], neonatal onset[12]
- Exact match: http://purl.obolibrary.org/obo/DOID_3672[13], http://identifiers.org/doid/DOID:3672[14]
- On focus list of Wikimedia project: WikiProject Medicine[15]
- Has phenotype: irritability[16], hematuria[17], arterial hypertension[18], weight loss[19], fever[20], Q141815132[21], abdominal pain[22], respiratory failure[23], headache[24], lymphadenopathy[25], cranial nerve palsy[26], kidney cancer[27], internal bleeding[28], oculomotor nerve paralysis[29]
- P14914: D69077[30]
Why It Matters
rhabdoid tumor is known by 8 alternative names across languages and contexts.[31]