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 49 28
Mild Androgen Insensitivity Syndrome 49
Undervirilized Male Syndrome 49
Mais 49

Classifications:



Summaries for Androgen Insensitivity Syndrome, Mild

MalaCards based summary : Androgen Insensitivity Syndrome, Mild, also known as mild androgen insensitivity syndrome, is related to may-hegglin anomaly and may-thurner syndrome.

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

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
16 ExPASy
18 FMA
27 GO
28 GTR
29 HGMD
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 MedGen
41 MeSH
42 MESH via Orphanet
43 MGI
45 NCI
46 NCIt
47 NDF-RT
50 NINDS
51 Novoseek
53 OMIM
54 OMIM via Orphanet
58 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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