MCID: AND005
MIFTS: 16

Androgen Insensitivity Syndrome, Mild

Categories: Rare diseases

Aliases & Classifications for Androgen Insensitivity Syndrome, Mild

MalaCards integrated aliases for Androgen Insensitivity Syndrome, Mild:

Name: Androgen Insensitivity Syndrome, Mild 53 29
Syndrome, Insensitivity, Androgen, Mild 40
Mild Androgen Insensitivity Syndrome 53
Undervirilized Male Syndrome 53
Mais 53

Classifications:



Summaries for Androgen Insensitivity Syndrome, Mild

MalaCards based summary : Androgen Insensitivity Syndrome, Mild, also known as syndrome, insensitivity, androgen, mild, is related to may-thurner syndrome and macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss.

Related Diseases for Androgen Insensitivity Syndrome, Mild

Diseases related to Androgen Insensitivity Syndrome, Mild via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 553, show less)
# Related Disease Score Top Affiliating Genes
1 may-thurner syndrome 12.3
2 macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 11.9
3 macs syndrome 11.3
4 myh9 related thrombocytopenia 11.3
5 prostate cancer 10.8
6 herpes zoster 10.8
7 crohn's disease 10.8
8 alzheimer disease 10.8
9 attention deficit-hyperactivity disorder 10.7
10 encephalitis 10.7
11 myocardial infarction 10.7
12 gastric cancer 10.7
13 breast cancer 10.7
14 lupus erythematosus 10.7
15 schizophrenia 10.7
16 dermatomyositis 10.7
17 multiple sclerosis 10.7
18 syringomyelia 10.7
19 epilepsy 10.7
20 premature ovarian failure 1 10.7
21 parkinson disease, late-onset 10.7
22 dermatitis 10.7
23 myeloma, multiple 10.7
24 myasthenia gravis 10.7
25 pancreatitis 10.7
26 graves' disease 10.7
27 dementia 10.7
28 vaginitis 10.7
29 chronic fatigue syndrome 10.7
30 leukemia, acute lymphoblastic 10.7
31 gastrointestinal stromal tumor 10.7
32 complex regional pain syndrome 10.7
33 esophagitis, eosinophilic, 1 10.7
34 leukemia, chronic lymphocytic 10.7
35 rheumatoid arthritis 10.7
36 autism spectrum disorder 10.7
37 hepatitis 10.7
38 spondyloarthropathy 1 10.7
39 pertussis 10.7
40 dyspepsia 10.7
41 ovarian cancer 10.7
42 cervical cancer 10.7
43 lyme disease 10.7
44 conn's syndrome 10.7
45 essential tremor 10.7
46 twin-to-twin transfusion syndrome 10.7
47 tonsillitis 10.7
48 thoracic outlet syndrome 10.7
49 chronic pain 10.7
50 hemophilia 10.6
51 fatty liver disease 10.6
52 paine syndrome 10.6
53 asthma 10.6
54 temporal arteritis 10.6
55 brittle bone disorder 10.6
56 agnosia 10.6
57 celiac disease 1 10.6
58 kawasaki disease 10.6
59 tardive dyskinesia 10.6
60 epidermolysis bullosa 10.6
61 narcolepsy 10.6
62 fainting 10.6
63 meningitis 10.6
64 leiomyoma, uterine 10.6
65 hypogonadotropic hypogonadism 10.6
66 palindromic rheumatism 10.6
67 diarrhea 10.6
68 neuroblastoma 10.6
69 hydrocephalus 10.6
70 peritonitis 10.6
71 leukemia 10.6
72 aneurysm 10.6
73 deficiency anemia 10.6
74 hereditary spastic paraplegia 10.6
75 apraxia 10.6
76 common cold 10.6
77 hypertrophic cardiomyopathy 10.6
78 traumatic brain injury 10.6
79 neural tube defects 10.6
80 atrial fibrillation 10.6
81 human immunodeficiency virus type 1 10.6
82 arachnoiditis 10.6
83 hypokalemic periodic paralysis, type 1 10.6
84 sickle cell disease 10.6
85 melanoma 10.6
86 colorectal cancer 10.6
87 down syndrome 10.6
88 influenza 10.6
89 muscular dystrophy 10.6
90 lymphoma 10.6
91 back pain 10.6
92 osteonecrosis 10.6
93 sleep apnea 10.6
94 factor vii deficiency 10.6
95 fabry disease 10.6
96 menkes disease 10.6
97 angina pectoris 10.6
98 gaucher's disease 10.6
99 myotonic dystrophy 10.6
100 multiple system atrophy 1 10.6
101 pulmonary fibrosis, idiopathic 10.6
102 interstitial cystitis 10.6
103 panic disorder 10.6
104 thalassemia 10.6
105 gastritis 10.6
106 pancreatic cancer 10.6
107 glioblastoma 10.6
108 diaphragmatic hernia, congenital 10.6
109 pneumothorax, primary spontaneous 10.6
110 gastroschisis 10.6
111 cerebral palsy 10.6
112 cholera 10.6
113 ovarian cyst 10.6
114 mercury poisoning 10.6
115 cataract 10.6
116 cystic fibrosis 10.6
117 esophageal cancer 10.6
118 beckwith-wiedemann syndrome 10.6
119 gilles de la tourette syndrome 10.6
120 butyrylcholinesterase deficiency 10.6
121 microcephaly 10.6
122 porphyria 10.6
123 erythromelalgia 10.6
124 hepatitis c 10.6
125 aortic aneurysm, familial abdominal, 1 10.6
126 lung cancer 10.6
127 bipolar disorder 10.6
128 vitamin b12 deficiency 10.6
129 dystonia 10.6
130 hemochromatosis, neonatal 10.6
131 leigh syndrome 10.6
132 microphthalmia 10.6
133 von willebrand's disease 10.6
134 nephrocalcinosis 10.6
135 myotonia congenita 10.6
136 chiari malformation 10.6
137 hepatitis b 10.6
138 squamous cell carcinoma 10.6
139 myelodysplastic syndrome 10.6
140 neuromyelitis optica 10.6
141 tremor 10.6
142 carpal tunnel syndrome 10.6
143 trigeminal neuralgia 10.6
144 ehlers-danlos syndrome 10.6
145 adult-onset still's disease 10.6
146 postpartum depression 10.6
147 polymyositis 10.6
148 syncope 10.6
149 b-cell lymphomas 10.6
150 hirschsprung disease 1 10.6
151 adenoid cystic carcinoma 10.6
152 lactose intolerance 10.6
153 craniopharyngioma 10.6
154 glomerulonephritis 10.6
155 acromegaly 10.6
156 anxiety 10.6
157 restless legs syndrome 10.6
158 hemochromatosis, type 1 10.6
159 panencephalitis, subacute sclerosing 10.6
160 neuroleptic malignant syndrome 10.6
161 cellulitis 10.6
162 rubella 10.6
163 autoimmune encephalitis 10.6
164 systemic onset juvenile idiopathic arthritis 10.6
165 transverse myelitis 10.6
166 periodontitis 10.6
167 optic nerve disease 10.6
168 headache 10.6
169 otitis media 10.6
170 myelofibrosis 10.6
171 sotos syndrome 1 10.5
172 holt-oram syndrome 10.5
173 buschke-ollendorff syndrome 10.5
174 joubert syndrome 1 10.5
175 melanosis, neurocutaneous 10.5
176 lymphangioleiomyomatosis 10.5
177 aortic valve disease 2 10.5
178 brugada syndrome 10.5
179 klippel-feil syndrome 10.5
180 cystic lymphangioma 10.5
181 reactive arthritis 10.5
182 acquired angioedema 10.5
183 nasopharyngitis 10.5
184 interstitial lung disease 10.5
185 polycystic ovary syndrome 10.5
186 heart disease 10.5
187 helicobacter pylori infection 10.5
188 craniosynostosis 10.5
189 diabetic neuropathy 10.5
190 tetanus 10.5
191 hereditary spherocytosis 10.5
192 diffuse large b-cell lymphoma 10.5
193 ulcerative colitis 10.5
194 exudative vitreoretinopathy 1 10.5
195 phenylketonuria 10.5
196 diphtheria 10.5
197 gastroparesis 10.5
198 food allergy 10.5
199 prion disease 10.5
200 macular degeneration, age-related, 1 10.5
201 polyneuropathy 10.5
202 osteoporosis 10.5
203 insulin-like growth factor i 10.5
204 fibromuscular dysplasia 10.5
205 cyclic vomiting syndrome 10.5
206 reflex sympathetic dystrophy 10.5
207 factor xi deficiency 10.5
208 porphyria, acute hepatic 10.5
209 charcot-marie-tooth disease 10.5
210 latex allergy 10.5
211 chagas disease 10.5
212 hepatitis a 10.5
213 guillain-barre syndrome 10.5
214 gout 10.5
215 tuberous sclerosis 10.5
216 causalgia 10.5
217 acute disseminated encephalomyelitis 10.5
218 juvenile rheumatoid arthritis 10.5
219 peptic ulcer disease 10.5
220 septic arthritis 10.5
221 brain injury 10.5
222 endocarditis 10.5
223 brucellosis 10.5
224 fibromyalgia 10.5
225 riboflavin deficiency 10.5
226 mycosis fungoides 10.5
227 aplastic anemia 10.5
228 cholangitis, primary sclerosing 10.5
229 chronic kidney failure 10.5
230 liver cirrhosis 10.5
231 spinal muscular atrophy 10.5
232 personality disorder 10.5
233 hypogonadism 10.5
234 irritable bowel syndrome 10.5
235 thyroid cancer, nonmedullary, 1 10.5
236 osteomyelitis 10.5
237 hepatic encephalopathy 10.5
238 peripheral nervous system disease 10.5
239 macroglossia 10.5
240 treacher collins syndrome 1 10.5
241 neurofibromatosis, type iv, of riccardi 10.5
242 ulnar-mammary syndrome 10.5
243 krabbe disease 10.5
244 budd-chiari syndrome 10.5
245 phelan-mcdermid syndrome 10.5
246 trichotillomania 10.5
247 west syndrome 10.5
248 osteopetrosis 10.5
249 waldenstrom macroglobulinemia 10.5
250 chikungunya 10.5
251 hepatic veno-occlusive disease 10.5
252 ankylosis 10.5
253 kernicterus 10.5
254 glucosephosphate dehydrogenase deficiency 10.5
255 cystic kidney disease 10.5
256 intestinal pseudo-obstruction 10.5
257 eccrine porocarcinoma 10.5
258 gigantism 10.5
259 pseudobulbar affect 10.5
260 thyrotoxic periodic paralysis 10.5
261 wells syndrome 10.5
262 hypersomnia 10.5
263 arthritis 10.5
264 diabetes mellitus, noninsulin-dependent 10.5
265 systemic lupus erythematosus 10.5
266 osteoarthritis 10.5
267 leukemia, chronic myeloid 10.5
268 peripheral artery disease 10.5
269 infective endocarditis 10.5
270 learning disability 10.5
271 dermatitis, atopic 10.5
272 huntington disease 10.5
273 hydrocephalus, normal-pressure 10.5
274 adenomyosis 10.5
275 cervical dystonia 10.5
276 bell's palsy 10.5
277 burning mouth syndrome 10.5
278 psoriasis 10.5
279 pemphigus 10.5
280 machado-joseph disease 10.5
281 polycythemia vera 10.5
282 acute promyelocytic leukemia 10.5
283 disseminated intravascular coagulation 10.5
284 liposarcoma 10.5
285 toxoplasmosis 10.5
286 arachnoid cysts 10.5
287 leukoplakia 10.5
288 head injury 10.5
289 whiplash 10.5
290 endometriosis 10.5
291 lymphoma, hodgkin, classic 10.5
292 coronary heart disease 1 10.5
293 dental caries 10.5
294 depression 10.5
295 major depressive disorder 10.5
296 pulmonary hypertension 10.5
297 vasculitis 10.5
298 adiposis dolorosa 10.5
299 van der woude syndrome 1 10.5
300 yellow nail syndrome 10.5
301 stiff-person syndrome 10.5
302 moyamoya disease 1 10.5
303 barth syndrome 10.5
304 supranuclear palsy, progressive, 1 10.5
305 breast reconstruction 10.5
306 chronic granulomatous disease 10.5
307 pemphigus vulgaris 10.5
308 thrombotic thrombocytopenic purpura 10.5
309 brain cancer 10.5
310 post-traumatic stress disorder 10.5
311 testicular cancer 10.5
312 nemaline myopathy 10.5
313 superior mesenteric artery syndrome 10.5
314 porokeratosis 10.5
315 chickenpox 10.5
316 aphthous stomatitis 10.5
317 linear porokeratosis 10.5
318 soft tissue sarcoma 10.5
319 amyotrophic lateral sclerosis 1 10.5
320 motor neuron disease 10.5
321 rosacea 10.5
322 hepatocellular carcinoma 10.5
323 constipation 10.5
324 bronchiolitis 10.5
325 encephalopathy 10.5
326 leukemia, acute myeloid 10.5
327 glioma 10.5
328 periodontal disease 10.5
329 polycystic kidney disease 10.5
330 cleidocranial dysplasia 10.5
331 lipomatosis, multiple symmetric 10.5
332 neurofibromatosis, type i 10.5
333 pityriasis rubra pilaris 10.5
334 testicular torsion 10.5
335 varicose veins 10.5
336 iron-refractory iron deficiency anemia 10.5
337 factor x deficiency 10.5
338 fanconi anemia, complementation group a 10.5
339 biotinidase deficiency 10.5
340 adrenoleukodystrophy 10.5
341 coats disease 10.5
342 sickle cell anemia 10.5
343 ewing sarcoma 10.5
344 keratoconus 10.5
345 myelodysplastic myeloproliferative cancer 10.5
346 myelomeningocele 10.5
347 depersonalization disorder 10.5
348 glossopharyngeal neuralgia 10.5
349 fallopian tube carcinoma 10.5
350 granular cell tumor 10.5
351 protein c deficiency 10.5
352 vaginal discharge 10.5
353 melorheostosis 10.5
354 prosopagnosia 10.5
355 epithelioid sarcoma 10.5
356 acral lentiginous melanoma 10.5
357 scabies 10.5
358 bullous pemphigoid 10.5
359 croup 10.5
360 median arcuate ligament syndrome 10.5
361 amniotic band syndrome 10.5
362 cor triatriatum sinister 10.5
363 malakoplakia 10.5
364 meralgia paresthetica 10.5
365 pemphigoid gestationis 10.5
366 talipes equinovarus 10.5
367 tracheobronchomalacia 10.5
368 tracheoesophageal fistula 10.5
369 myotonia 10.5
370 pneumonia 10.5
371 inclusion body myositis 10.5
372 retinal detachment 10.5
373 pulmonary disease, chronic obstructive 10.5
374 chlamydia 10.5
375 optic neuritis 10.5
376 hidradenitis suppurativa 10.5
377 thymoma 10.5
378 teratoma 10.5
379 hypoglycemia 10.5
380 bladder cancer 10.5
381 thrombosis 10.5
382 prostatic hyperplasia, benign 10.5
383 psoriatic arthritis 10.5
384 beta-thalassemia 10.5
385 coccidioidomycosis 10.5
386 schistosomiasis 10.5
387 impotence 10.5
388 long qt syndrome 10.5
389 conjunctivitis 10.5
390 diverticulitis 10.5
391 hyperthyroidism 10.5
392 myoclonus 10.5
393 graft-versus-host disease 10.4
394 migraine with or without aura 1 10.4
395 dermatofibrosarcoma protuberans 10.4
396 sinusitis 10.4
397 ectopic pregnancy 10.4
398 lemierre's syndrome 10.4
399 rift valley fever 10.4
400 candidiasis 10.4
401 essential thrombocythemia 10.4
402 iga glomerulonephritis 10.4
403 turner syndrome 10.4
404 gastric adenocarcinoma 10.4
405 merkel cell carcinoma 10.4
406 perinatal necrotizing enterocolitis 10.4
407 malaria 10.4
408 myositis 10.4
409 kidney disease 10.4
410 friedreich ataxia 1 10.4
411 rett syndrome 10.4
412 langerhans cell histiocytosis 10.4
413 paroxysmal nocturnal hemoglobinuria 10.4
414 spinal cord injury 10.4
415 intracranial aneurysm 10.4
416 syphilis 10.4
417 avian influenza 10.4
418 myocarditis 10.4
419 charles bonnet syndrome 10.4
420 cluster headache 10.4
421 hemicrania continua 10.4
422 limbic encephalitis 10.4
423 cervicitis 10.4
424 marfan syndrome 10.4
425 benign chronic pemphigus 10.4
426 lipoid congenital adrenal hyperplasia 10.4
427 squamous cell carcinoma, head and neck 10.4
428 alcoholic liver cirrhosis 10.4
429 holoprosencephaly 10.4
430 lissencephaly 10.4
431 zollinger-ellison syndrome 10.4
432 leukodystrophy 10.4
433 hellp syndrome 10.4
434 echinococcosis 10.4
435 disease of mental health 10.4
436 kidney cancer 10.4
437 hepatoblastoma 10.4
438 aortic coarctation 10.4
439 brittle diabetes 10.4
440 chronic thromboembolic pulmonary hypertension 10.4
441 igg4-related disease 10.4
442 mollaret meningitis 10.4
443 pancreatic neuroendocrine tumor 10.4
444 pulmonary arteriovenous malformation 10.4
445 retroperitoneal fibrosis 10.4
446 cytomegalovirus infection 10.4
447 developmental dyspraxia 10.4
448 paresthesia 10.4
449 cleft lip/palate 10.4
450 spasticity 10.4
451 male infertility 10.4
452 patent foramen ovale 10.4
453 hypothyroidism 10.4
454 acute pancreatitis 10.4
455 autonomic dysfunction 10.4
456 colitis 10.4
457 sclerosing cholangitis 10.4
458 poliomyelitis 10.4
459 oral cancer 10.4
460 burkitt lymphoma 10.4
461 cleft palate, isolated 10.4
462 klippel-trenaunay-weber syndrome 10.4
463 pernicious anemia 10.4
464 peyronie disease 10.4
465 mccune-albright syndrome 10.4
466 exfoliation syndrome 10.4
467 pulmonary atresia with ventricular septal defect 10.4
468 arthrogryposis, distal, type 2a 10.4
469 wilms tumor 1 10.4
470 anemia, autoimmune hemolytic 10.4
471 acth-independent macronodular adrenal hyperplasia 10.4
472 neurodegeneration with brain iron accumulation 1 10.4
473 hypothalamic hamartomas 10.4
474 lipoid proteinosis of urbach and wiethe 10.4
475 myopathy, congenital 10.4
476 pierre robin syndrome 10.4
477 pulmonary alveolar microlithiasis 10.4
478 ichthyosis, x-linked 10.4
479 androgen insensitivity, partial 10.4
480 glaucoma-related pigment dispersion syndrome 10.4
481 autoimmune lymphoproliferative syndrome 10.4
482 alpha-thalassemia 10.4
483 bulimia nervosa 10.4
484 melioidosis 10.4
485 nevus comedonicus 10.4
486 hemophagocytic lymphohistiocytosis 10.4
487 collagenous colitis 10.4
488 robinow syndrome 10.4
489 peeling skin syndrome 10.4
490 kleefstra syndrome 10.4
491 catecholaminergic polymorphic ventricular tachycardia 10.4
492 cysticercosis 10.4
493 sleeping sickness 10.4
494 cat-scratch disease 10.4
495 onchocerciasis 10.4
496 oral candidiasis 10.4
497 rheumatic fever 10.4
498 transient cerebral ischemia 10.4
499 bursitis 10.4
500 inverted papilloma 10.4
501 mixed connective tissue disease 10.4
502 agoraphobia 10.4
503 zellweger syndrome 10.4
504 trichinosis 10.4
505 refractive error 10.4
506 anaplastic thyroid cancer 10.4
507 ciguatera fish poisoning 10.4
508 congenital cytomegalovirus 10.4
509 fibrosing mediastinitis 10.4
510 frontal fibrosing alopecia 10.4
511 hemiplegic migraine 10.4
512 notalgia paresthetica 10.4
513 pulmonary arterio-veinous fistula 10.4
514 pulmonary sequestration 10.4
515 synovial chondromatosis 10.4
516 central precocious puberty 10.4
517 angiomatosis 10.4
518 cerebral aneurysms 10.4
519 hereditary neuropathies 10.4
520 megalencephaly 10.4
521 lung cancer susceptibility 3 10.4
522 dilated cardiomyopathy 10.4
523 retinitis 10.4
524 familial mediterranean fever 10.4
525 aspergillosis 10.4
526 nephrotic syndrome 10.4
527 relapsing-remitting multiple sclerosis 10.4
528 malignant hyperthermia 10.4
529 gastroesophageal reflux 10.4
530 prader-willi syndrome 10.4
531 vesicoureteral reflux 1 10.4
532 bronchiolitis obliterans 10.4
533 focal segmental glomerulosclerosis 10.4
534 legionnaires' disease 10.4
535 primary hyperparathyroidism 10.4
536 hemolytic-uremic syndrome 10.4
537 autosomal dominant cerebellar ataxia 10.4
538 pulmonary embolism 10.4
539 thrombocytopenic purpura, autoimmune 10.4
540 fragile x syndrome 10.4
541 alcoholic hepatitis 10.4
542 pulmonary fibrosis 10.4
543 pre-eclampsia 10.4
544 dracunculiasis 10.4
545 pneumothorax 10.4
546 basal cell carcinoma 10.4
547 dyslexia 10.4
548 vascular dementia 10.4
549 dysphagia 10.4
550 sturge-weber syndrome 10.4
551 adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 10.4
552 wiskott-aldrich syndrome 10.4
553 androgen insensitivity syndrome 9.9

Graphical network of the top 20 diseases related to Androgen Insensitivity Syndrome, Mild:



Diseases related to Androgen Insensitivity Syndrome, Mild

Symptoms & Phenotypes for Androgen Insensitivity Syndrome, Mild

Drugs & Therapeutics for Androgen Insensitivity Syndrome, Mild

Search Clinical Trials , NIH Clinical Center for Androgen Insensitivity Syndrome, Mild

Genetic Tests for Androgen Insensitivity Syndrome, Mild

Genetic tests related to Androgen Insensitivity Syndrome, Mild:

# Genetic test Affiliating Genes
1 Androgen Insensitivity Syndrome, Mild 29

Anatomical Context for Androgen Insensitivity Syndrome, Mild

Publications for Androgen Insensitivity Syndrome, Mild

Articles related to Androgen Insensitivity Syndrome, Mild:

(showing 3, show less)
# Title Authors Year
1
Mild androgen insensitivity syndrome (MAIS): the identification of c.1783C>T mutation in two unrelated infertile men. ( 28659371 )
2017
2
Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation. ( 22469007 )
2012
3
Identification of a novel mutation in exon 1 ofA androgen receptor gene in an azoospermic patientA with mild androgen insensitivity syndrome: case report and literature review. ( 21962961 )
2011

Variations for Androgen Insensitivity Syndrome, Mild

Expression for Androgen Insensitivity Syndrome, Mild

Search GEO for disease gene expression data for Androgen Insensitivity Syndrome, Mild.

Pathways for Androgen Insensitivity Syndrome, Mild

GO Terms for Androgen Insensitivity Syndrome, Mild

Sources for Androgen Insensitivity Syndrome, Mild

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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