Simpson-Golabi-Behmel syndrome

Summary

Simpson-Golabi-Behmel syndrome is a head and neck disease^[1]. It draws 72 Wikipedia views per month (head_and_neck_disease category, ranking #30 of 92).^[2]

Key Facts

• Simpson-Golabi-Behmel syndrome's instance of is recorded as head and neck disease^[3].
• Simpson-Golabi-Behmel syndrome's instance of is recorded as developmental defect during embryogenesis^[4].
• Simpson-Golabi-Behmel syndrome's instance of is recorded as rare disease^[5].
• Simpson-Golabi-Behmel syndrome's instance of is recorded as class of disease^[6].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as overgrowth syndrome^[7].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as rare genetic bone disease^[8].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as polymalformative genetic syndrome with increased risk of developing cancer^[9].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as syndromic renal or urinary tract malformation^[10].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as X-linked intellectual disability^[11].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability^[12].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as syndromic diaphragmatic or abdominal wall malformation^[13].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as macroglossia^[14].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as syndrome or malformation associated with head and neck malformations^[15].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as syndromic diaphragmatic or thoracic malformation^[16].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as X-linked recessive disease^[17].
• Simpson-Golabi-Behmel syndrome's subclass of is recorded as syndrome^[18].
• Simpson-Golabi-Behmel syndrome's MeSH descriptor ID is recorded as C537340^[19].
• Simpson-Golabi-Behmel syndrome's OMIM ID is recorded as 312870^[20].
• Simpson-Golabi-Behmel syndrome's ICD-10 ID is recorded as Q87.0^[21].
• Simpson-Golabi-Behmel syndrome's DiseasesDB is recorded as 32640^[22].
• Simpson-Golabi-Behmel syndrome's Freebase ID is recorded as /m/0bmrfz^[23].
• Simpson-Golabi-Behmel syndrome's KEGG ID is recorded as H01215^[24].
• Simpson-Golabi-Behmel syndrome's Disease Ontology ID is recorded as DOID:0060248^[25].
• Simpson-Golabi-Behmel syndrome's Orphanet ID is recorded as 373^[26].
• Simpson-Golabi-Behmel syndrome's ICD-9-CM is recorded as 759.89^[27].

Why It Matters

Simpson-Golabi-Behmel syndrome draws 72 Wikipedia views per month (head_and_neck_disease category, ranking #30 of 92).^[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.^[28] It is known by 18 alternative names across languages and contexts.^[29]