creatine transporter deficiency

Summary

creatine transporter deficiency is a developmental defect during embryogenesis^[1]. It draws 336 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).^[2]

Key Facts

• creatine transporter deficiency's instance of is recorded as developmental defect during embryogenesis^[3].
• creatine transporter deficiency's instance of is recorded as rare disease^[4].
• creatine transporter deficiency's instance of is recorded as class of disease^[5].
• creatine transporter deficiency is a type of cerebral creatine deficiency syndrome^[6].
• creatine transporter deficiency is a type of syndromic neurometabolic disease with X-linked intellectual disability^[7].
• creatine transporter deficiency is a type of developmental anomaly of metabolic origin^[8].
• creatine transporter deficiency is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability^[9].
• creatine transporter deficiency's ICD-9-CM is recorded as 758.81^[10].
• creatine transporter deficiency's NCI Thesaurus ID is recorded as C125665^[11].
• creatine transporter deficiency's health specialty is recorded as medical genetics^[12].
• creatine transporter deficiency's genetic association is recorded as SLC6A8^[13].
• creatine transporter deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050800^[14].
• creatine transporter deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0050800^[15].
• creatine transporter deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_52503^[16].
• creatine transporter deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].

Why It Matters

creatine transporter deficiency draws 336 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).^[2] It is known by 17 alternative names across languages and contexts.^[18]