Nicolaides–Baraitser syndrome
medical condition
Press Enter · cited answer in seconds
0 sources
Nicolaides–Baraitser syndrome
Summary
Nicolaides–Baraitser syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Nicolaides–Baraitser syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Nicolaides–Baraitser syndrome's instance of is recorded as rare disease[4].
- Nicolaides–Baraitser syndrome's instance of is recorded as class of disease[5].
- Nicolaides–Baraitser syndrome is a type of syndromic intellectual disability[6].
- Nicolaides–Baraitser syndrome is a type of genetic syndromic intellectual disability[7].
- Nicolaides–Baraitser syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- Nicolaides–Baraitser syndrome's Commons category is recorded as Nicolaides-Baraitser syndrome[9].
- Nicolaides–Baraitser syndrome's NCI Thesaurus ID is recorded as C205644[10].
- Nicolaides–Baraitser syndrome's genetic association is recorded as SMARCA2[11].
- Nicolaides–Baraitser syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3051[12].
Why It Matters
Nicolaides–Baraitser syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 7 alternative names across languages and contexts.[13]