RGD Annotation Report for Kallmann Syndrome 5Rat Genome Database

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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13814243 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:25741868 PMID:28492532 PMID:32870266

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8642727 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:18073582 PMID:21158681 PMID:22033296 PMID:22461308 PMID:22539353 PMID:24033266 PMID:25741868 PMID:25931334 PMID:28492532 PMID:29255181

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:9682224 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:18414213 PMID:21158681 PMID:24033266 PMID:25077900 PMID:25741868 PMID:28492532 PMID:32870266

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12836890 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:22033296 PMID:22461308 PMID:22539353 PMID:25741868 PMID:28492532

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11347163 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:22539353 PMID:25741868 PMID:28492532

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8642714 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:23885230 PMID:25741868 PMID:28492532

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens) & RGD:10045020\|RGD:10050375\|RGD:10404139\|RGD:11645742\|RGD:11653966\|RGD:11654698\|RGD:126919947\|RGD:127322834\|RGD:12846358\|RGD:12847986\|RGD:13469182\|RGD:13472771\|RGD:13538034\|RGD:13617874\|RGD:13617880\|RGD:13812021\|RGD:13828456\|RGD:13828588\|RGD:14701723\|RGD:14704004\|RGD:14714067\|RGD:14716057\|RGD:150411427\|RGD:150417893\|RGD:150551778\|RGD:15173860\|RGD:151833101\|RGD:152085338\|RGD:28868616\|RGD:8642704\|RGD:8642711\|RGD:8642717\|RGD:8642723 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8642708 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:15300250 PMID:16155193 PMID:16615981 PMID:21158681 PMID:21931733 PMID:22033296 PMID:22461308 PMID:25741868 PMID:28492532 PMID:29255276

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10052017\|RGD:11642671\|RGD:11647316\|RGD:13515727\|RGD:15146494 (Homo sapiens) & RGD:10052017\|RGD:11642671\|RGD:11647316\|RGD:13515727\|RGD:15146494 (Homo sapiens) & RGD:10052017\|RGD:11642671\|RGD:11647316\|RGD:13515727\|RGD:15146494 (Homo sapiens) & RGD:10052017\|RGD:11642671\|RGD:11647316\|RGD:13515727\|RGD:15146494 (Homo sapiens) & RGD:10052017\|RGD:11642671\|RGD:11647316\|RGD:13515727\|RGD:15146494 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:24033266 PMID:25741868 PMID:28492532

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11645611 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:30311386

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10052824 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:22461308 PMID:22539353 PMID:24033266 PMID:25741868 PMID:28492532

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10048182\|RGD:15161657 (Homo sapiens) & RGD:10048182\|RGD:15161657 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11648509 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:22461308 PMID:25741868 PMID:28492532 PMID:30311386

An association has been curated linking CHD7 and Kallmann Syndrome 5 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8569994 (Homo sapiens)
1 RGD objects have been annotated to Kallmann Syndrome 5 (DOID:9003232)
13 papers in RGD have been used to annotate CHD7
Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 5
Original References(s): PMID:17576681 PMID:18834967 PMID:25741868 PMID:28492532 PMID:29419413 PMID:30311386 PMID:34837038 PMID:9536098

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GENE - TERM ANNOTATION REPORT

14 Annotations Found.