Bannayan-Riley-Ruvalcaba syndrome
a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas.
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Bannayan-Riley-Ruvalcaba syndrome
Summary
Bannayan-Riley-Ruvalcaba syndrome is a developmental defect during embryogenesis[1]. It draws 17 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #124 of 308).[2]
Key Facts
- Bannayan-Riley-Ruvalcaba syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Bannayan-Riley-Ruvalcaba syndrome's instance of is recorded as rare disease[4].
- Bannayan-Riley-Ruvalcaba syndrome's instance of is recorded as class of disease[5].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as autosomal dominant disease[6].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as multiple hamartoma syndrome[7].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as inherited digestive tract tumor[8].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as rare genetic vascular tumor[9].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as brain cancer[10].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as complex vascular malformation with associated anomalies[11].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as rare nervous system tumor[12].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[13].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as genetic syndromic intellectual disability[14].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as genetic skin vascular disorder[15].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as overgrowth syndrome[16].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as penile disease[17].
- Bannayan-Riley-Ruvalcaba syndrome's subclass of is recorded as syndrome[18].
- Bannayan-Riley-Ruvalcaba syndrome's OMIM ID is recorded as 158350[19].
- Bannayan-Riley-Ruvalcaba syndrome's DiseasesDB is recorded as 31337[20].
- Bannayan-Riley-Ruvalcaba syndrome's Freebase ID is recorded as /m/0bdch8[21].
- Bannayan-Riley-Ruvalcaba syndrome's GeneReviews ID is recorded as NBK1488[22].
- Bannayan-Riley-Ruvalcaba syndrome's Disease Ontology ID is recorded as DOID:0050657[23].
- Bannayan-Riley-Ruvalcaba syndrome's Orphanet ID is recorded as 109[24].
- Bannayan-Riley-Ruvalcaba syndrome's ICD-9-CM is recorded as 759.6[25].
- Bannayan-Riley-Ruvalcaba syndrome's NCI Thesaurus ID is recorded as C3939[26].
- Bannayan-Riley-Ruvalcaba syndrome's health specialty is recorded as oncology[27].
Why It Matters
Bannayan-Riley-Ruvalcaba syndrome draws 17 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #124 of 308).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] It is known by 27 alternative names across languages and contexts.[29]