RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: androgen insensitivity syndrome
Accession: DOID:4674
browse the term
Definition: A disorder of sexual development that is characterized by the inability of the cell to respond to androgens in individuals with a karyotype of 46,XY resulting in female physical traits but male genetic makeup. (DO)
Synonyms: exact_synonym: AIS; AR Deficiencies; AR Deficiency; Androgen Receptor Deficiency; Androgen Resistance Syndrome; DHTR Deficiencies; DHTR Deficiency; Dihydrotestosterone Receptor Deficiencies; Dihydrotestosterone Receptor Deficiency; Feminisation - testicular; Goldberg-Maxwell syndrome; Male Pseudohermaphroditism Due to Androgen Insensitivity; TFM; Testicular Feminization; androgen insensitivity syndromes; androgen receptor deficiencies; androgen resistance syndromes; testicular feminization syndrome; testicular feminization syndromes; testicular feminizations
primary_id: MESH:D013734
alt_id: MIM:300068
xref: GARD:5803 ; ICD10CM:E34.5 ; ICD9CM:259.51 ; NCI:C120191 ; NCI:C27226 ; ORDO:754
For additional species annotation, visit the
Alliance of Genome Resources .
G
Ar
androgen receptor
susceptibility
ISO ISS IEP
CTD Direct Evidence: marker/mechanism ClinVar Annotator: match by term: Androgen resistance syndrome | ClinVar Annotator: match by term: Dihydrotestosterone receptor deficiency OMIM:300068 DNA:missense mutation:exon:p.M749V (human) DNA:missense mutations, repeats:exon:p.V866L, p.R607Y (human) DNA:missense mutation:exon:p.R615S (human) DNA:point mutation, repeats:exon DNA:deletion protein:altered localization:spinal cord, motor neuron, cytoplasm
CTD OMIM ClinVar MouseDO RGD
PMID:1158706 PMID:1303262 PMID:1307250 PMID:1430233 PMID:1458719 PMID:1480178 PMID:1487249 PMID:1508223 PMID:1569163 PMID:1598912 PMID:1609793 PMID:1631125 PMID:1720929 PMID:1750490 PMID:1752359 PMID:1775137 PMID:1779964 PMID:2082179 PMID:2293020 PMID:2332504 PMID:2339702 PMID:2594783 PMID:3174628 PMID:3186717 PMID:3216866 PMID:4061484 PMID:7537149 PMID:7581399 PMID:7626493 PMID:7633398 PMID:7641413 PMID:7671849 PMID:7723794 PMID:7795646 PMID:7910529 PMID:7970939 PMID:7981687 PMID:7981689 PMID:8033918 PMID:8040309 PMID:8096390 PMID:8097257 PMID:8126121 PMID:8162033 PMID:8224266 PMID:8281139 PMID:8325932 PMID:8413310 PMID:8450040 PMID:8450042 PMID:8530589 PMID:8626869 PMID:8628719 PMID:8647313 PMID:8723113 PMID:8809734 PMID:8823308 PMID:8824883 PMID:8990010 PMID:9007482 PMID:9039340 PMID:9196614 PMID:9302173 PMID:9328206 PMID:9332480 PMID:9360511 PMID:9463997 PMID:9536098 PMID:9543136 PMID:9544375 PMID:9554754 PMID:9576916 PMID:9627582 PMID:9698822 PMID:9768671 PMID:9788719 PMID:9851768 PMID:9856504 PMID:9921903 PMID:10022458 PMID:10092153 PMID:10221692 PMID:10221770 PMID:10323251 PMID:10323385 PMID:10359561 PMID:10425033 PMID:10458483 PMID:10502786 PMID:10571951 PMID:10589774 PMID:10690872 PMID:10834333 PMID:10840043 PMID:10852459 PMID:10946887 PMID:11103816 PMID:11181525 PMID:11225909 PMID:11260228 PMID:11376111 PMID:11397856 PMID:11549642 PMID:11579211 PMID:11744994 PMID:11788616 PMID:11788645 PMID:11788673 PMID:11889162 PMID:12068007 PMID:12213902 PMID:12466388 PMID:12644579 PMID:12705360 PMID:12843171 PMID:13680382 PMID:14701682 PMID:14974091 PMID:15109605 PMID:15266301 PMID:15531547 PMID:15541764 PMID:15925895 PMID:15963062 PMID:16083860 PMID:16199547 PMID:16283146 PMID:16365032 PMID:16373394 PMID:16450583 PMID:16470553 PMID:16804045 PMID:17161333 PMID:17382127 PMID:17576681 PMID:17937062 PMID:17970778 PMID:18406699 PMID:18710728 PMID:19463997 PMID:20007693 PMID:20011049 PMID:20056211 PMID:20150575 PMID:20305676 PMID:20493947 PMID:20671138 PMID:21520333 PMID:21645389 PMID:21710452 PMID:21962961 PMID:22334387 PMID:22403669 PMID:22412043 PMID:22995991 PMID:23106833 PMID:23637914 PMID:23774508 PMID:23779130 PMID:24033266 PMID:24186138 PMID:24321103 PMID:24367986 PMID:24737579 PMID:24790346 PMID:25241384 PMID:25248670 PMID:25299611 PMID:25326637 PMID:25433660 PMID:25500996 PMID:25613104 PMID:25640679 PMID:25674389 PMID:25740850 PMID:25741868 PMID:26303084 PMID:26688387 PMID:26778393 PMID:26806084 PMID:26813233 PMID:26980296 PMID:27051040 PMID:27267075 PMID:27284311 PMID:27403927 PMID:27583472 PMID:27849622 PMID:27854360 PMID:27899157 PMID:27989800 PMID:28186600 PMID:28261839 PMID:28456808 PMID:28492532 PMID:28611373 PMID:28624954 PMID:28659371 PMID:28743543 PMID:28857053 PMID:28879700 PMID:28947719 PMID:29051026 PMID:29237170 PMID:29758562 PMID:29785970 PMID:30064134 PMID:30113450 PMID:30165367 PMID:30316867 PMID:30401990 PMID:30599484 PMID:30668521 PMID:30815925 PMID:31012339 PMID:31180159 PMID:31219235 PMID:31373714 PMID:31429517 PMID:31499074 PMID:31871297 PMID:32229106 PMID:32345305 PMID:32985417 PMID:33505695 PMID:33514065 PMID:33548461 PMID:33728612 PMID:33750429 PMID:33819955 PMID:33863387 PMID:34152287 PMID:34276780 PMID:34333495 PMID:34689141 PMID:35445939 PMID:35561789 PMID:35809576 PMID:36394509 PMID:36572623 PMID:1487249 PMID:8325950 PMID:1424203 PMID:20888558 PMID:7970939 PMID:3186717 PMID:7643075 More...
RGD:11576240 , RGD:11576235 , RGD:11576233 , RGD:11576232 , RGD:11571628 , RGD:11571627 , RGD:11571622
NCBI chr X:63,104,771...63,273,934
Ensembl chr X:63,104,771...63,273,925
G
Cdc45
cell division cycle 45
ISO
ClinVar Annotator: match by term: Dihydrotestosterone receptor deficiency
ClinVar
PMID:25741868 PMID:28492532
NCBI chr11:82,185,427...82,210,630
Ensembl chr11:82,185,473...82,210,619
G
Fkbp4
FKBP prolyl isomerase 4
ISS
OMIM:300068
MouseDO
NCBI chr 4:161,703,379...161,711,833
Ensembl chr 4:161,703,379...161,711,833
G
Kat7
lysine acetyltransferase 7
ISO
protein:decreased expression:testes (human)
RGD
PMID:23707616
RGD:9681005
NCBI chr10:80,221,519...80,255,590
Ensembl chr10:80,221,524...80,255,567
G
Ar
androgen receptor
ISO
ClinVar Annotator: match by term: Androgen insensitivity syndrome due to coactivator deficiency
ClinVar
PMID:2594783 PMID:9544375 PMID:10852459 PMID:16804045 PMID:17970778 PMID:22403669 PMID:22412043 PMID:23637914 PMID:25299611 PMID:25326637 PMID:25500996 PMID:25740850 PMID:25741868 PMID:26688387 PMID:26806084 PMID:27583472 PMID:27899157 PMID:28492532 PMID:28611373 PMID:28624954 PMID:28659371 PMID:30599484 PMID:31871297 PMID:36572623 More...
NCBI chr X:63,104,771...63,273,934
Ensembl chr X:63,104,771...63,273,925
G
Cdc45
cell division cycle 45
ISO
ClinVar Annotator: match by term: Androgen insensitivity syndrome due to coactivator deficiency
ClinVar
PMID:25741868 PMID:28492532
NCBI chr11:82,185,427...82,210,630
Ensembl chr11:82,185,473...82,210,619
G
Ar
androgen receptor
ISO
ClinVar Annotator: match by term: Type I familial incomplete male pseudohermaphroditism
ClinVar
PMID:2594783 PMID:16804045 PMID:25326637 PMID:25740850 PMID:25741868 PMID:26688387 PMID:26806084 PMID:27583472 PMID:28492532 PMID:36572623 More...
NCBI chr X:63,104,771...63,273,934
Ensembl chr X:63,104,771...63,273,925
G
Ar
androgen receptor
susceptibility
ISO
ClinVar Annotator: match by term: Androgen insensitivity, partial, with breast cancer | ClinVar Annotator: match by term: Partial androgen insensitivity syndrome | ClinVar Annotator: match by term: Reifenstein syndrome
ClinVar OMIM
PMID:1303262 PMID:1307250 PMID:1430233 PMID:1598912 PMID:2010552 PMID:2594783 PMID:2918059 PMID:7581399 PMID:7671849 PMID:8040309 PMID:8096390 PMID:8097257 PMID:8281139 PMID:8325932 PMID:8446106 PMID:8628719 PMID:8723113 PMID:8823308 PMID:8824883 PMID:9345099 PMID:9543136 PMID:9768671 PMID:9851768 PMID:9856504 PMID:9921903 PMID:10221692 PMID:10485299 PMID:10502786 PMID:10543676 PMID:10946887 PMID:10999818 PMID:11788616 PMID:11788673 PMID:15001585 PMID:15109605 PMID:15925895 PMID:16083860 PMID:16450583 PMID:16804045 PMID:20011049 PMID:23808476 PMID:24321103 PMID:24737579 PMID:25241384 PMID:25326637 PMID:25740850 PMID:25741868 PMID:26688387 PMID:26778393 PMID:26806084 PMID:27267075 PMID:27583472 PMID:28186600 PMID:28261839 PMID:28492532 PMID:28624954 PMID:29237170 PMID:30668521 PMID:32985417 PMID:33750429 PMID:36572623 More...
NCBI chr X:63,104,771...63,273,934
Ensembl chr X:63,104,771...63,273,925
G
Gli2
GLI family zinc finger 2
ISO
ClinVar Annotator: match by term: Partial androgen insensitivity syndrome
ClinVar
PMID:19223936 PMID:21204792 PMID:22967285 PMID:23408573 PMID:25741868 PMID:28492532 More...
NCBI chr13:29,946,882...30,163,589
Ensembl chr13:29,946,809...30,163,574
Term paths to the root one shortest all shortest one longest all longest one shortest and longest all