cephalocele

Summary

cephalocele is a developmental defect during embryogenesis^[1].

Key Facts

• cephalocele's instance of is recorded as developmental defect during embryogenesis^[2].
• cephalocele's instance of is recorded as class of disease^[3].
• cephalocele's subclass of is recorded as neural tube defect^[4].
• cephalocele's Orphanet ID is recorded as 268817^[5].
• cephalocele's ICD-9-CM is recorded as 742.0^[6].
• cephalocele's Google Knowledge Graph ID is recorded as /g/1hh_pjd2b^[7].
• cephalocele's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_268817^[8].
• cephalocele's UMLS CUI is recorded as C0014065^[9].
• cephalocele's Human Phenotype Ontology ID is recorded as HP:0011815^[10].
• cephalocele's ICD-10-CM is recorded as Q01.8^[11].
• cephalocele's ICD-10-CM is recorded as Q01.1^[12].
• cephalocele's ICD-10-CM is recorded as Q01.2^[13].
• cephalocele's ICD-10-CM is recorded as Q01.0^[14].
• cephalocele's ICD-10-CM is recorded as Q01.9^[15].
• cephalocele's Mondo ID is recorded as MONDO_0017078^[16].
• cephalocele's ICD-11 ID is recorded as LA01^[17].
• cephalocele's ICD-11 ID is recorded as 1520916568^[18].