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 35 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's subclass of is recorded as syndrome[6].
- KBG syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- KBG syndrome's subclass of is recorded as malformation syndrome with odontal and/or periodontal component[8].
- KBG syndrome's subclass of is recorded as genetic syndromic intellectual disability[9].
- KBG syndrome's subclass of is recorded as spinal disease[10].
- KBG syndrome's Commons category is recorded as KBG syndrome[11].
- KBG syndrome's MeSH descriptor ID is recorded as C537015[12].
- KBG syndrome's OMIM ID is recorded as 148050[13].
- KBG syndrome's KEGG ID is recorded as H02327[14].
- KBG syndrome's Disease Ontology ID is recorded as DOID:14780[15].
- KBG syndrome's Orphanet ID is recorded as 2332[16].
- KBG syndrome's ICD-9-CM is recorded as 759.89[17].
- KBG syndrome's genetic association is recorded as ANKRD11[18].
- KBG syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14780[19].
- KBG syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14780[20].
- KBG syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2332[21].
- KBG syndrome's UMLS CUI is recorded as C0220687[22].
- KBG syndrome's ICD-10-CM is recorded as Q87.8[23].
- KBG syndrome's GARD rare disease ID is recorded as 82[24].
- KBG syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[25].
- KBG syndrome's Mondo ID is recorded as MONDO_0007846[26].
- KBG syndrome's SNOMED CT ID is recorded as 711156009[27].
Why It Matters
KBG syndrome draws 35 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.[28] It is known by 8 alternative names across languages and contexts.[29]