Seckel syndrome
autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability
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Seckel syndrome
Summary
Seckel syndrome is a rare disease[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Seckel syndrome's instance of is recorded as rare disease[3].
- Seckel syndrome's instance of is recorded as class of disease[4].
- Seckel syndrome is a type of autosomal recessive disease[5].
- Seckel syndrome is a type of primordial dwarfism[6].
- Seckel syndrome is a type of syndrome[7].
- Seckel syndrome is a type of disease[8].
- Seckel syndrome's NCI Thesaurus ID is recorded as C125488[9].
- Seckel syndrome's health specialty is recorded as medical genetics[10].
- Seckel syndrome's genetic association is recorded as ATR[11].
- Seckel syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050569[12].
- Seckel syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050569[13].
- Seckel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_808[14].
- Seckel syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
Seckel syndrome has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[16]