Jackson–Weiss syndrome
disease
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Jackson–Weiss syndrome
Summary
Jackson–Weiss syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Jackson–Weiss syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Jackson–Weiss syndrome's instance of is recorded as class of disease[4].
- Jackson–Weiss syndrome is a type of craniosynostosis[5].
- Jackson–Weiss syndrome is a type of autosomal recessive disease[6].
- Jackson–Weiss syndrome is a type of syndrome[7].
- Jackson–Weiss syndrome's ICD-9-CM is recorded as 759.89[8].
- Jackson–Weiss syndrome's NCI Thesaurus ID is recorded as C123814[9].
- Jackson–Weiss syndrome's genetic association is recorded as FGFR1[10].
- Jackson–Weiss syndrome's genetic association is recorded as FGFR2[11].
- Jackson–Weiss syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1540[12].
- Jackson–Weiss syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111337[13].
- Jackson–Weiss syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111337[14].
Why It Matters
Jackson–Weiss syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 6 alternative names across languages and contexts.[15]