DOID:0080014

Name:	chromosomal disease
Namespace:	disease_ontology

Ontology association<br>Each term has an is_a parent in the Disease Ontology, which has a linkage to an another entity and FANTOM5 samples.Libraries were grouped into mutually exclusive facets according to the FANTOM5 sample ontology mapping to DISEASE ontologies.<br><br>link to ontology dataset<br>data

---

Parents

is_a:	DOID:0050177(monogenic disease)

Children

is a:	DOID:11983 (Prader-Willi syndrome),DOID:14250 (Down syndrome),DOID:14447 (gonadal dysgenesis)

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Human (Homo sapiens)

• 10521-107E8
• 10804-111A3
• 10806-111A5
• 10814-111B4
• 13445-144F7 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
• 13446-144F8 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
• 13447-144F9 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
• 13448-144G1 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
• 13449-144G2 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
• 13450-144G3 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)

... further results Mouse (Mus musculus)

• 10521-107E8
• 10804-111A3
• 10806-111A5
• 10814-111B4
• 13445-144F7 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
• 13446-144F8 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
• 13447-144F9 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
• 13448-144G1 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
• 13449-144G2 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
• 13450-144G3 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)

... further results

Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:0080014 (chromosomal disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data

---

No analysis results