KBG syndrome
syndrome that is characterized by short stature, moderate to severe degrees of mental retardation, developmental abnormalities of the limbs, bones of the spine (vertebrae), extremities, and/or underdevelopment of the bones of the skeleton
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KBG syndrome
Summary
KBG syndrome is a developmental defect during embryogenesis[1]. It draws 154 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #114 of 308).[2]
Key Facts
- KBG syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- KBG syndrome's instance of is recorded as rare disease[4].
- KBG syndrome's instance of is recorded as class of disease[5].
- KBG syndrome is a type of syndrome[6].
- KBG syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- KBG syndrome is a type of malformation syndrome with odontal and/or periodontal component[8].
- KBG syndrome is a type of genetic syndromic intellectual disability[9].
- KBG syndrome is a type of spinal disease[10].
- KBG syndrome's Commons category is recorded as KBG syndrome[11].
- KBG syndrome's ICD-9-CM is recorded as 759.89[12].
- KBG syndrome's genetic association is recorded as ANKRD11[13].
- KBG syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14780[14].
- KBG syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14780[15].
- KBG syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2332[16].
- KBG syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
KBG syndrome draws 154 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #114 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[18] It is known by 8 alternative names across languages and contexts.[19]