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{
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"results": [
{
"accession": "CLO:0031684",
"name": "GM14611 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0031663",
"name": "GM14609 cell",
"definition": "[' HPS1 GENE; HPS1 HERMANSKY-PUDLAK SYNDROME; HPS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031664",
"name": "GM14606 cell",
"definition": "[' HPS1 GENE; HPS1 HERMANSKY-PUDLAK SYNDROME; HPS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031661",
"name": "GM14599 cell",
"definition": "[' CHROMOSOME 6 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031662",
"name": "GM14593 cell",
"definition": "[' MONOZYGOTIC TWIN PAIRS APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031659",
"name": "GM14592 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS MONOZYGOTIC TWIN PAIRS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031660",
"name": "GM14590 cell",
"definition": "[' COCKAYNE SYNDROME, TYPE I; CKN1']",
"term_type": "cell line"
},
{
"accession": "CLO:0031667",
"name": "GM14589 cell",
"definition": "[' COCKAYNE SYNDROME, TYPE I; CKN1']",
"term_type": "cell line"
},
{
"accession": "CLO:0031668",
"name": "GM14584 cell",
"definition": "[' NON-OBESE CONTROLS APPARENTLY HEALTHY NON-FETAL TISSUE MONOZYGOTIC TWIN PAIRS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031665",
"name": "GM14583 cell",
"definition": "[' MONOZYGOTIC TWIN PAIRS APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031666",
"name": "GM14582 cell",
"definition": "[' MONOZYGOTIC TWIN PAIRS APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031585",
"name": "GM14581 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS MONOZYGOTIC TWIN PAIRS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031584",
"name": "GM14579 cell",
"definition": "[' TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0031583",
"name": "GM14577 cell",
"definition": "[' TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0031582",
"name": "GM14576 cell",
"definition": "[' TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0031581",
"name": "GM14569 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE MONOZYGOTIC TWIN PAIRS NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031580",
"name": "GM14568 cell",
"definition": "[' MONOZYGOTIC TWIN PAIRS APPARENTLY HEALTHY NON-FETAL TISSUE NON-OBESE CONTROLS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031579",
"name": "GM14566 cell",
"definition": "[' CHROMOSOME 18 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031578",
"name": "GM14565 cell",
"definition": "[' CHROMOSOME 18 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031577",
"name": "GM14564 cell",
"definition": "[' CHROMOSOME 18 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
}
]
}