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 ranks in the top 2% of rare_disease entities by monthly Wikipedia readership (1,246 views/month).[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's subclass of is recorded as autosomal recessive disease[5].
- Seckel syndrome's subclass of is recorded as primordial dwarfism[6].
- Seckel syndrome's subclass of is recorded as syndrome[7].
- Seckel syndrome's subclass of is recorded as disease[8].
- Seckel syndrome's OMIM ID is recorded as 210600[9].
- Seckel syndrome's ICD-9 ID is recorded as 759.89[10].
- Seckel syndrome's DiseasesDB is recorded as 31625[11].
- Seckel syndrome's Freebase ID is recorded as /m/0cd6h_[12].
- Seckel syndrome's KEGG ID is recorded as H00992[13].
- Seckel syndrome's Disease Ontology ID is recorded as DOID:0050569[14].
- Seckel syndrome's Orphanet ID is recorded as 808[15].
- Seckel syndrome's NCI Thesaurus ID is recorded as C125488[16].
- Seckel syndrome's health specialty is recorded as medical genetics[17].
- Seckel syndrome's genetic association is recorded as ATR[18].
- Seckel syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050569[19].
- Seckel syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050569[20].
- Seckel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_808[21].
- Seckel syndrome's ICD-10-CM is recorded as Q87.1[22].
- Seckel syndrome's GARD rare disease ID is recorded as 8562[23].
- Seckel syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].
- Seckel syndrome's Microsoft Academic ID is recorded as 2778565148[25].
- Seckel syndrome's WikiProjectMed ID is recorded as Seckel syndrome[26].
Why It Matters
Seckel syndrome ranks in the top 2% of rare_disease entities by monthly Wikipedia readership (1,246 views/month).[2] It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[27] It is known by 8 alternative names across languages and contexts.[28]