chromosome 1p32-p31 deletion syndrome
Human disease
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chromosome 1p32-p31 deletion syndrome
Summary
chromosome 1p32-p31 deletion syndrome is a developmental defect during embryogenesis[1].
Key Facts
- chromosome 1p32-p31 deletion syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- chromosome 1p32-p31 deletion syndrome's instance of is recorded as class of disease[3].
- chromosome 1p32-p31 deletion syndrome is a type of chromosomal deletion syndrome[4].
- chromosome 1p32-p31 deletion syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[5].
- chromosome 1p32-p31 deletion syndrome is a type of partial deletion of the short arm of chromosome 1[6].
- chromosome 1p32-p31 deletion syndrome is a type of syndrome[7].
- chromosome 1p32-p31 deletion syndrome is a type of autosomal dominant disease[8].
- chromosome 1p32-p31 deletion syndrome's health specialty is recorded as medical genetics[9].
- chromosome 1p32-p31 deletion syndrome's genetic association is recorded as NFIA[10].
- chromosome 1p32-p31 deletion syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060409[11].
- chromosome 1p32-p31 deletion syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060409[12].
- chromosome 1p32-p31 deletion syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_401986[13].
- chromosome 1p32-p31 deletion syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].