chromosome 1q21.1 deletion syndrome
Human disease
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chromosome 1q21.1 deletion syndrome
Summary
chromosome 1q21.1 deletion 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
- chromosome 1q21.1 deletion syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- chromosome 1q21.1 deletion syndrome's instance of is recorded as class of disease[4].
- chromosome 1q21.1 deletion syndrome is a type of chromosomal deletion syndrome[5].
- chromosome 1q21.1 deletion syndrome is a type of 1q21.1 copy number variations[6].
- chromosome 1q21.1 deletion syndrome is a type of partial deletion of the long arm of chromosome 1[7].
- chromosome 1q21.1 deletion syndrome's mode of inheritance is recorded as autosomal dominant[8].
- chromosome 1q21.1 deletion syndrome's ICD-9-CM is recorded as 758.33[9].
- chromosome 1q21.1 deletion syndrome's health specialty is recorded as medical genetics[10].
- chromosome 1q21.1 deletion syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060411[11].
- chromosome 1q21.1 deletion syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060411[12].
- chromosome 1q21.1 deletion syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_250989[13].
- chromosome 1q21.1 deletion syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
chromosome 1q21.1 deletion syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 4 alternative names across languages and contexts.[15]