<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR988/004/ERR9888084/ERR9888084_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/001/ERR9896531/ERR9896531.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/002/ERR9896532/ERR9896532.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/005/ERR9890755/ERR9890755_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR988/004/ERR9888084/ERR9888084_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/003/ERR9896533/ERR9896533.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/005/ERR9890755/ERR9890755_2.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Max Planck Institute for Evolutionary Anthropology</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJEB53912</full_dataset_link><long_description>The Greek colony of Himera lasted from 648 BCE until its destruction by Carthage in 409 BCE and is one of the most extensively excavated cities from the Greek archaic / classical world. The skeletal remains belonging to a single male individual showing morphological indications of dwarfism were found in 2009 in the Western Necropolis of Himera in Sicily. Genetic analysis of genome-wide data generated for this individual confirmed the diagnosis of achondroplasia. This individual had entirely Anatolian ancestry.</long_description><repository>ENA</repository><name_synonyms>"Chondrodystrophia" EXACT [MTHICD9_2006:756.4], "Achondroplasia (disorder)" EXACT [SNOMEDCT_2005_07_31:86268005], Skeleton Skin Brain Syndrome, Skeleton-Skin-Brain Syndromes, set of bones of body, Skeleton-Skin-Brain, "Achondroplastic physique" EXACT [SNOMEDCT_2005_07_31:190584003], SADDAN Dysplasia, SADDAN Dysplasias, determination, Skeleton-Skin-Brain Syndrome, skeleton, Skeletons, Set of all bones, "Achondroplastic dwarf" EXACT [SNOMEDCT_2005_07_31:205467007], Dysplasias, Dysplasia, Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans, ACH, skeleton component, Syndromes, set of all bones, "osteosclerosis congenita" EXACT [CSP2005:2715-2940], SADDAN, "achondroplasia" EXACT [CSP2005:1849-0171]., chemical analysis, Syndrome, "Achondroplastic dwarf" EXACT [SNOMEDCT_2005_07_31:268273004], Achondroplasias, Achondroplasia, Achondroplastic dwarfism, With Developmental Delay And Acanthosis Nigricans, assay, "Achondroplastic physique (finding)" EXACT [SNOMEDCT_2005_07_31:248299001], SADDANs, Severe, Skelettsystem, Skeleton (in vivo), Set of bones of body</name_synonyms></additional><is_claimable>false</is_claimable><name>Genomic analysis of 5th century BCE skeleton from Himera, Sicily, reveals confirmed case of achondroplasia</name><description>An achondroplastic individual from 5 th century BCE Himera, Sicily</description><dates><last_updated>2024-06-04</last_updated><first_public>2024-06-04</first_public></dates><accession>PRJEB53912</accession><cross_references/></HashMap>