Simpson-Golabi-Behmel syndrome
X-linked disease characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities
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Simpson-Golabi-Behmel syndrome
Summary
Simpson-Golabi-Behmel syndrome is a head and neck disease[1]. It draws 169 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 is a type of overgrowth syndrome[7].
- Simpson-Golabi-Behmel syndrome is a type of rare genetic bone disease[8].
- Simpson-Golabi-Behmel syndrome is a type of polymalformative genetic syndrome with increased risk of developing cancer[9].
- Simpson-Golabi-Behmel syndrome is a type of syndromic renal or urinary tract malformation[10].
- Simpson-Golabi-Behmel syndrome is a type of X-linked intellectual disability[11].
- Simpson-Golabi-Behmel syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[12].
- Simpson-Golabi-Behmel syndrome is a type of syndromic diaphragmatic or abdominal wall malformation[13].
- Simpson-Golabi-Behmel syndrome is a type of macroglossia[14].
- Simpson-Golabi-Behmel syndrome is a type of syndrome or malformation associated with head and neck malformations[15].
- Simpson-Golabi-Behmel syndrome is a type of syndromic diaphragmatic or thoracic malformation[16].
- Simpson-Golabi-Behmel syndrome is a type of X-linked recessive disease[17].
- Simpson-Golabi-Behmel syndrome is a type of syndrome[18].
- Simpson-Golabi-Behmel syndrome's ICD-9-CM is recorded as 759.89[19].
- Simpson-Golabi-Behmel syndrome's NCI Thesaurus ID is recorded as C131002[20].
- Simpson-Golabi-Behmel syndrome's NCI Thesaurus ID is recorded as C118787[21].
- Simpson-Golabi-Behmel syndrome's health specialty is recorded as medical genetics[22].
- Simpson-Golabi-Behmel syndrome's genetic association is recorded as GPC3[23].
- Simpson-Golabi-Behmel syndrome's genetic association is recorded as OFD1[24].
- Simpson-Golabi-Behmel syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060248[25].
- Simpson-Golabi-Behmel syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060248[26].
- Simpson-Golabi-Behmel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_373[27].
Why It Matters
Simpson-Golabi-Behmel syndrome draws 169 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]