ERS
MCID: AML006
MIFTS: 21

Amelogenesis Imperfecta Hypoplastic Type, Ig (ERS)

Categories: Metabolic diseases, Nephrological diseases, Oral diseases, Rare diseases

Aliases & Classifications for Amelogenesis Imperfecta Hypoplastic Type, Ig

MalaCards integrated aliases for Amelogenesis Imperfecta Hypoplastic Type, Ig:

Name: Amelogenesis Imperfecta Hypoplastic Type, Ig 52
Amelogenesis Imperfecta Nephrocalcinosis 52 71
Absent Enamel, Nephrocalcinosis and Apparently Normal Calcium Metabolism 52
Generalized Enamel Hypoplasia and Renal Dysfunction 52
Amelogenesis Imperfecta and Nephrocalcinosis 52
Enamel-Renal Syndrome 52
Enamel Renal Syndrome 52
Ai1g 52
Ers 52

Classifications:



External Ids:

UMLS 71 C2931783

Summaries for Amelogenesis Imperfecta Hypoplastic Type, Ig

NIH Rare Diseases : 52 The following summary is from Orphanet , a European reference portal for information on rare diseases and orphan drugs. Orpha Number: 1031 Definition A extremely rare, genetic malformation syndrome characterized by hypoplastic amelogenesis imperfecta (hypoplastic dental enamel) and nephrocalcinosis (precipitation of calcium salts in renal tissue ). Oral manifestations include yellow and misshaped teeth, delayed tooth eruption, and intrapulpal calcifications. Nephrocalcinosis is often asymptomatic but can progress during late childhood or early adulthood to impaired renal function, recurrent urinary infections, renal tubular acidosis, and rarely to end-stage renal failure. Visit the Orphanet disease page for more resources.

MalaCards based summary : Amelogenesis Imperfecta Hypoplastic Type, Ig, also known as amelogenesis imperfecta nephrocalcinosis, is related to epithelial recurrent erosion dystrophy and estrogen resistance, and has symptoms including polyuria Affiliated tissues include breast, lung and kidney.

Related Diseases for Amelogenesis Imperfecta Hypoplastic Type, Ig

Diseases in the Hypoplastic Amelogenesis Imperfecta family:

Amelogenesis Imperfecta Hypoplastic Type, Ig

Diseases related to Amelogenesis Imperfecta Hypoplastic Type, Ig via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 1068, show less)
# Related Disease Score Top Affiliating Genes
1 epithelial recurrent erosion dystrophy 12.2
2 estrogen resistance 11.6
3 breast cancer 11.6
4 amelogenesis imperfecta, type ig 11.6
5 alzheimer disease 11.5
6 idiopathic interstitial pneumonia 11.5
7 atherosclerosis susceptibility 11.5
8 marinesco-sjogren syndrome 11.4
9 coronary heart disease 1 11.4
10 factor v and factor viii, combined deficiency of, 1 11.4
11 muscular dystrophy, congenital, lmna-related 11.4
12 deafness, dystonia, and cerebral hypomyelination 11.3
13 congenital disorder of glycosylation, type ik 11.3
14 epidermodysplasia verruciformis 1 11.1
15 cerebellar atrophy, visual impairment, and psychomotor retardation 11.1
16 peripheral vascular disease 11.1
17 nephrocalcinosis 10.5
18 amelogenesis imperfecta 10.5
19 adenocarcinoma 10.4
20 lung cancer susceptibility 3 10.4
21 amyotrophic lateral sclerosis 1 10.4
22 lateral sclerosis 10.4
23 endometrial cancer 10.4
24 fatty liver disease, nonalcoholic 1 10.4
25 periodontitis 10.4
26 fatty liver disease 10.4
27 neuroblastoma 10.3
28 polykaryocytosis inducer 10.3
29 stomatitis 10.3
30 autosomal recessive disease 10.3
31 gingival fibromatosis 10.3
32 fibromatosis 10.3
33 non-alcoholic fatty liver disease 10.3
34 lung disease 10.3
35 hepatocellular carcinoma 10.3
36 periodontitis, chronic 10.2
37 dowling-degos disease 1 10.2
38 b-cell lymphoma 10.2
39 in situ carcinoma 10.2
40 colorectal cancer 10.2
41 ovarian cancer 10.2
42 triiodothyronine receptor auxiliary protein 10.2
43 hyperglycemia 10.2
44 pulmonary fibrosis 10.2
45 ductal carcinoma in situ 10.2
46 depression 10.2
47 mental depression 10.2
48 prostate cancer 10.2
49 lung cancer 10.2
50 major depressive disorder 10.2
51 glioblastoma multiforme 10.2
52 glioma 10.2
53 helix syndrome 10.2
54 adenocarcinoma in situ 10.2
55 glial tumor 10.2
56 neurofibromatosis, type ii 10.2
57 rapidly involuting congenital hemangioma 10.2
58 pulmonary hypertension 10.2
59 inflammatory bowel disease 10.2
60 huntington disease 10.1
61 pulmonary fibrosis, idiopathic 10.1
62 liver disease 10.1
63 nephrolithiasis, calcium oxalate 10.1
64 hypogonadism-cataract syndrome 10.1
65 wolfram syndrome 1 10.1
66 myeloma, multiple 10.1
67 glucose intolerance 10.1
68 gingival recession 10.1
69 retinal degeneration 10.1
70 osteoporosis 10.1
71 osteogenic sarcoma 10.1
72 paraplegia 10.1
73 hypertension, essential 10.1
74 gastric cancer 10.1
75 pachyonychia congenita 3 10.1
76 estrogen-receptor positive breast cancer 10.1
77 allergic hypersensitivity disease 10.1
78 breast ductal carcinoma 10.1
79 ischemia 10.1
80 hypoxia 10.1
81 autoimmune disease 10.1
82 body mass index quantitative trait locus 11 10.1
83 pulmonary disease, chronic obstructive 10.1
84 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.1
85 non-alcoholic steatohepatitis 10.1
86 wolfram syndrome 10.1
87 interstitial lung disease 10.1
88 insulinoma 10.1
89 chronic pain 10.1
90 pancreatic cancer 10.1
91 retinitis pigmentosa 10.1
92 insulin-like growth factor i 10.1
93 hepatitis c virus 10.1
94 neuroretinitis 10.1
95 lymphocytic leukemia 10.1
96 dental caries 10.1
97 hereditary spastic paraplegia 10.1
98 endometriosis 10.1
99 lipid metabolism disorder 10.1
100 retinitis 10.1
101 myopathy 10.1
102 neuropathy 10.1
103 body mass index quantitative trait locus 9 10.1
104 body mass index quantitative trait locus 8 10.1
105 body mass index quantitative trait locus 4 10.1
106 body mass index quantitative trait locus 10 10.1
107 body mass index quantitative trait locus 7 10.1
108 body mass index quantitative trait locus 12 10.1
109 body mass index quantitative trait locus 14 10.1
110 body mass index quantitative trait locus 18 10.1
111 body mass index quantitative trait locus 19 10.1
112 body mass index quantitative trait locus 20 10.1
113 bone resorption disease 10.1
114 melanoma 10.1
115 constipation 10.1
116 parkinson disease, late-onset 10.1
117 cystic fibrosis 10.1
118 microvascular complications of diabetes 3 10.1
119 microvascular complications of diabetes 4 10.1
120 microvascular complications of diabetes 6 10.1
121 microvascular complications of diabetes 7 10.1
122 48,xyyy 10.1
123 bone mineral density quantitative trait locus 8 10.0
124 bone mineral density quantitative trait locus 15 10.0
125 low compliance bladder 10.0
126 breast adenocarcinoma 10.0
127 myocarditis 10.0
128 osteoarthritis 10.0
129 ataxia and polyneuropathy, adult-onset 10.0
130 major affective disorder 8 10.0
131 major affective disorder 9 10.0
132 dengue virus 10.0
133 exanthem 10.0
134 bipolar disorder 10.0
135 hypoglycemia 10.0
136 pulmonary hypertension, primary, 1 10.0
137 cervical cancer 10.0
138 endometrial hyperplasia 10.0
139 cerebral artery occlusion 10.0
140 kidney disease 10.0
141 peripheral nervous system disease 10.0
142 bronchitis 10.0
143 prion disease 10.0
144 diabetes insipidus 10.0
145 hair whorl 10.0
146 alacrima, achalasia, and mental retardation syndrome 10.0
147 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.0
148 mucopolysaccharidosis-plus syndrome 10.0
149 nonsyndromic deafness 10.0
150 hypercementosis 10.0
151 root resorption 10.0
152 hypertrichosis 10.0
153 hypoplastic amelogenesis imperfecta 10.0
154 atrial standstill 1 10.0
155 retinoblastoma 10.0
156 open-angle glaucoma 10.0
157 cholera 10.0
158 vascular disease 10.0
159 hepatitis c 10.0
160 endometrial adenocarcinoma 10.0
161 familial retinoblastoma 10.0
162 chronic kidney disease 10.0
163 brain injury 10.0
164 encephalopathy 10.0
165 spinal cord injury 10.0
166 fibrosis of extraocular muscles, congenital, 1 9.9
167 small cell cancer of the lung 9.9
168 microvascular complications of diabetes 5 9.9
169 ectodermal dysplasia-syndactyly syndrome 2 9.9
170 oral squamous cell carcinoma 9.9
171 osteonecrosis 9.9
172 japanese encephalitis 9.9
173 diarrhea 9.9
174 squamous cell carcinoma 9.9
175 acute pancreatitis 9.9
176 severe combined immunodeficiency 9.9
177 crohn's disease 9.9
178 bronchiectasis 9.9
179 alopecia 9.9
180 cytokine deficiency 9.9
181 back pain 9.9
182 thrombotic microangiopathy 9.9
183 glaucoma, primary open angle 9.9
184 renal cell carcinoma, nonpapillary 9.9
185 leukemia, chronic lymphocytic 9.9
186 branchiootic syndrome 1 9.9
187 macular degeneration, age-related, 1 9.9
188 homocysteinemia 9.9
189 brittle bone disorder 9.9
190 body mass index quantitative trait locus 1 9.9
191 intraocular pressure quantitative trait locus 9.9
192 leukemia, acute lymphoblastic 9.9
193 hypertrophic scars 9.9
194 female breast cancer 9.9
195 charcot-marie-tooth disease 9.9
196 respiratory failure 9.9
197 neutropenia 9.9
198 gaucher's disease 9.9
199 motor neuron disease 9.9
200 bronchiolitis 9.9
201 bronchiolo-alveolar adenocarcinoma 9.9
202 muscular atrophy 9.9
203 sporadic breast cancer 9.9
204 47,xyy 9.9
205 spastic paraplegia 3a 9.9
206 spasticity 9.9
207 thyroid carcinoma 9.9
208 hypercholesterolemia, familial, 1 9.9
209 lentigines 9.9
210 metaphyseal chondrodysplasia, schmid type 9.9
211 sarcoidosis 1 9.9
212 spastic paraplegia 3, autosomal dominant 9.9
213 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 9.9
214 frontotemporal dementia 9.9
215 anxiety 9.9
216 renal fibrosis 9.9
217 lymphoma 9.9
218 bacterial infectious disease 9.9
219 dentin caries 9.9
220 thrombotic thrombocytopenic purpura 9.9
221 tooth disease 9.9
222 prostatic hypertrophy 9.9
223 telangiectasis 9.9
224 cholestasis 9.9
225 neuronal ceroid lipofuscinosis 9.9
226 kidney cancer 9.9
227 mucinous adenocarcinoma 9.9
228 astrocytoma 9.9
229 purpura 9.9
230 pancreatic ductal adenocarcinoma 9.9
231 appendix adenocarcinoma 9.9
232 hemolytic anemia 9.9
233 ulcerative colitis 9.9
234 encephalitis 9.9
235 allergic encephalomyelitis 9.9
236 leukoplakia 9.9
237 traumatic brain injury 9.9
238 alcohol dependence 9.8
239 papillomatosis, confluent and reticulated 9.8
240 suppressor of tumorigenicity 3 9.8
241 ataxia-telangiectasia 9.8
242 ceroid storage disease 9.8
243 schopf-schulz-passarge syndrome 9.8
244 gaucher disease, type i 9.8
245 3-methylglutaconic aciduria, type iii 9.8
246 aging 9.8
247 prostatic hyperplasia, benign 9.8
248 leukemia, acute lymphoblastic 3 9.8
249 neuronal ceroid-lipofuscinoses 9.8
250 pertussis 9.8
251 visual epilepsy 9.8
252 dilated cardiomyopathy 9.8
253 tuberous sclerosis 9.8
254 estrogen excess 9.8
255 alcohol use disorder 9.8
256 impotence 9.8
257 benign mesothelioma 9.8
258 bronchiolitis obliterans 9.8
259 long qt syndrome 9.8
260 prostatic adenoma 9.8
261 lysosomal storage disease 9.8
262 ureteral obstruction 9.8
263 retinal disease 9.8
264 cataract 9.8
265 herpes simplex 9.8
266 amyloidosis 9.8
267 muscular dystrophy 9.8
268 oral leukoplakia 9.8
269 seizure disorder 9.8
270 manganese poisoning 9.8
271 osteonecrosis of the jaw 9.8
272 diabetes mellitus, noninsulin-dependent 9.8
273 multiple sclerosis 9.8
274 attention deficit-hyperactivity disorder 9.8
275 hypertriglyceridemia, familial 9.8
276 rheumatoid arthritis 9.8
277 schizophrenia 9.8
278 tuberous sclerosis 1 9.8
279 arterial calcification, generalized, of infancy, 1 9.8
280 proteasome-associated autoinflammatory syndrome 1 9.8
281 ceroid lipofuscinosis, neuronal, 8 9.8
282 wilms tumor 5 9.8
283 yemenite deaf-blind hypopigmentation syndrome 9.8
284 legionnaire disease 9.8
285 human immunodeficiency virus type 1 9.8
286 acute promyelocytic leukemia 9.8
287 aspergillosis 9.8
288 familial adenomatous polyposis 9.8
289 hereditary sensory neuropathy 9.8
290 diffuse large b-cell lymphoma 9.8
291 sleep apnea 9.8
292 sexual disorder 9.8
293 colitis 9.8
294 early-onset parkinson's disease 9.8
295 adenoid cystic carcinoma 9.8
296 opioid abuse 9.8
297 autonomic neuropathy 9.8
298 leukemia 9.8
299 toxic shock syndrome 9.8
300 hypothyroidism 9.8
301 keratosis 9.8
302 breast fibroadenoma 9.8
303 status epilepticus 9.8
304 hyperuricemia 9.8
305 enamel erosion 9.8
306 corneal dystrophy 9.8
307 papilloma 9.8
308 breast disease 9.8
309 mouth disease 9.8
310 liver cirrhosis 9.8
311 dystonia 9.8
312 adenoma 9.8
313 cerebrovascular disease 9.8
314 active peptic ulcer disease 9.8
315 lupus erythematosus 9.8
316 skin melanoma 9.8
317 diabetes mellitus 9.8
318 pulmonary fibrosis, familial 9.8
319 erythrokeratoderma ''en cocardes'' 9.8
320 oral cancer 9.8
321 ovarian epithelial cancer 9.8
322 pyogenic granuloma 9.8
323 myoclonus 9.8
324 pituitary tumors 9.8
325 tremor 9.8
326 obsolete: squamous cell carcinoma of head and neck 9.8
327 ankyloglossia with or without tooth anomalies 9.7
328 bladder cancer 9.7
329 diabetes insipidus, neurohypophyseal 9.7
330 diabetes insipidus, nephrogenic, autosomal 9.7
331 dystonia 1, torsion, autosomal dominant 9.7
332 kaposi sarcoma 9.7
333 leiomyoma, uterine 9.7
334 migraine with or without aura 1 9.7
335 thyroid cancer, nonmedullary, 1 9.7
336 down syndrome 9.7
337 vitiligo-associated multiple autoimmune disease susceptibility 6 9.7
338 abetalipoproteinemia 9.7
339 adrenocortical carcinoma, hereditary 9.7
340 autism 9.7
341 bronchomalacia 9.7
342 epiphyseal dysplasia, multiple, with early-onset diabetes mellitus 9.7
343 ocular motor apraxia 9.7
344 alopecia, androgenetic, 2 9.7
345 asthma 9.7
346 stroke, ischemic 9.7
347 patent ductus venosus 9.7
348 leukemia, acute myeloid 9.7
349 malignant atrophic papulosis 9.7
350 meningioma, radiation-induced 9.7
351 vitiligo-associated multiple autoimmune disease susceptibility 1 9.7
352 nasopharyngeal carcinoma 9.7
353 myocardial infarction 9.7
354 amyotrophic lateral sclerosis 8 9.7
355 spastic paraplegia 31, autosomal dominant 9.7
356 alpha-1-antitrypsin deficiency 9.7
357 myelodysplastic syndrome 9.7
358 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 9.7
359 angina pectoris 9.7
360 adrenal cortical carcinoma 9.7
361 invasive aspergillosis 9.7
362 oculocutaneous albinism 9.7
363 mantle cell lymphoma 9.7
364 estrogen-receptor negative breast cancer 9.7
365 dowling-degos disease 9.7
366 tracheomalacia 9.7
367 cardiac arrest 9.7
368 thrombosis 9.7
369 coronavirus infection 9.7
370 sleeping sickness 9.7
371 hand, foot and mouth disease 9.7
372 chlamydia 9.7
373 endometriosis of ovary 9.7
374 goiter 9.7
375 leiomyoma 9.7
376 multiple epiphyseal dysplasia 9.7
377 dementia 9.7
378 hypoactive sexual desire disorder 9.7
379 squamous cell papilloma 9.7
380 root caries 9.7
381 generalized anxiety disorder 9.7
382 aggressive periodontitis 9.7
383 optic nerve disease 9.7
384 hyperinsulinism 9.7
385 post-traumatic stress disorder 9.7
386 sensory peripheral neuropathy 9.7
387 basal cell carcinoma 9.7
388 hemangioma 9.7
389 nonspecific interstitial pneumonia 9.7
390 glomerulonephritis 9.7
391 severe acute respiratory syndrome 9.7
392 acute kidney failure 9.7
393 malignant glioma 9.7
394 cystadenocarcinoma 9.7
395 serous cystadenocarcinoma 9.7
396 teratocarcinoma 9.7
397 mood disorder 9.7
398 cervical adenocarcinoma 9.7
399 pituitary adenoma 9.7
400 adrenal cortical adenocarcinoma 9.7
401 thyroid gland papillary carcinoma 9.7
402 carcinosarcoma 9.7
403 clear cell renal cell carcinoma 9.7
404 pancreatitis 9.7
405 eye disease 9.7
406 ovarian serous cystadenocarcinoma 9.7
407 uterine corpus serous adenocarcinoma 9.7
408 panic disorder 9.7
409 congestive heart failure 9.7
410 acute stress disorder 9.7
411 overnutrition 9.7
412 peritonitis 9.7
413 myeloid leukemia 9.7
414 pulmonary embolism 9.7
415 yellow fever 9.7
416 diabetic neuropathy 9.7
417 albinism 9.7
418 candida glabrata 9.7
419 dentinogenesis imperfecta type 2 9.7
420 lymphoma aids related 9.7
421 dysphagia 9.7
422 posttransplant acute limbic encephalitis 9.7
423 acute liver failure 9.7
424 precursor t-cell acute lymphoblastic leukemia 9.7
425 alopecia, androgenetic, 1 9.6
426 schnyder corneal dystrophy 9.6
427 lenz-majewski hyperostotic dwarfism 9.6
428 systemic lupus erythematosus 9.6
429 mesothelioma, malignant 9.6
430 antigen defined by monoclonal antibody aj9 9.6
431 myositis 9.6
432 obsessive-compulsive disorder 9.6
433 otitis media 9.6
434 benign chronic pemphigus 9.6
435 pheochromocytoma 9.6
436 scleroderma, familial progressive 9.6
437 thrombophilia due to thrombin defect 9.6
438 tangier disease 9.6
439 camptodactyly syndrome, guadalajara, type i 9.6
440 celiac disease 1 9.6
441 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.6
442 hemochromatosis, type 1 9.6
443 lymphoma, hodgkin, classic 9.6
444 hypoadrenocorticism, familial 9.6
445 lymphoid interstitial pneumonia 9.6
446 short-rib thoracic dysplasia 6 with or without polydactyly 9.6
447 peeling skin syndrome 1 9.6
448 thymoma, familial 9.6
449 46,xy sex reversal 2 9.6
450 muscular dystrophy, duchenne type 9.6
451 pituitary adenoma, prolactin-secreting 9.6
452 suppression of tumorigenicity 12 9.6
453 encephalopathy, familial, with neuroserpin inclusion bodies 9.6
454 aceruloplasminemia 9.6
455 spastic paraplegia 12, autosomal dominant 9.6
456 wolfram syndrome 2 9.6
457 lymphoma, non-hodgkin, familial 9.6
458 kufor-rakeb syndrome 9.6
459 bone mineral density quantitative trait locus 3 9.6
460 creatinine clearance quantitative trait locus 9.6
461 meningioma, familial 9.6
462 mammographic density 9.6
463 bulimia nervosa 9.6
464 kala-azar 1 9.6
465 west nile virus 9.6
466 buruli ulcer 9.6
467 factor v and factor viii, combined deficiency of, 2 9.6
468 long qt syndrome 2 9.6
469 myopia, high, with cataract and vitreoretinal degeneration 9.6
470 spastic paraplegia 61, autosomal recessive 9.6
471 chorea, childhood-onset, with psychomotor retardation 9.6
472 chronic ulcer of skin 9.6
473 chikungunya 9.6
474 multinodular goiter 9.6
475 adult t-cell leukemia 9.6
476 androgenic alopecia 9.6
477 fibroma 9.6
478 adrenal gland pheochromocytoma 9.6
479 ovarian serous carcinoma 9.6
480 autism spectrum disorder 9.6
481 cutaneous t cell lymphoma 9.6
482 crohn's colitis 9.6
483 ptosis 9.6
484 mucositis 9.6
485 sensorineural hearing loss 9.6
486 common cold 9.6
487 leukodystrophy 9.6
488 pre-eclampsia 9.6
489 hypertrophy of breast 9.6
490 mastitis 9.6
491 pulpitis 9.6
492 anogenital venereal wart 9.6
493 social phobia 9.6
494 chronic apical periodontitis 9.6
495 spinal meningioma 9.6
496 heart disease 9.6
497 infant gynecomastia 9.6
498 presbyopia 9.6
499 gestational diabetes 9.6
500 myopia 9.6
501 nephrotic syndrome 9.6
502 gastroparesis 9.6
503 chagas disease 9.6
504 common variable immunodeficiency 9.6
505 otosclerosis 9.6
506 dengue disease 9.6
507 paranoid schizophrenia 9.6
508 male infertility 9.6
509 spinal muscular atrophy 9.6
510 dysentery 9.6
511 acute leukemia 9.6
512 gynecomastia 9.6
513 choreatic disease 9.6
514 cardiovascular system disease 9.6
515 mucocele of salivary gland 9.6
516 alcoholic cardiomyopathy 9.6
517 focal segmental glomerulosclerosis 9.6
518 dental fluorosis 9.6
519 familial hypercholesterolemia 9.6
520 achromatopsia 9.6
521 autosomal dominant cerebellar ataxia 9.6
522 dumping syndrome 9.6
523 personality disorder 9.6
524 rheumatic disease 9.6
525 thrombocytopenia 9.6
526 pneumothorax 9.6
527 cheilitis 9.6
528 enthesopathy 9.6
529 hepatitis b 9.6
530 enamel caries 9.6
531 iron metabolism disease 9.6
532 kernicterus 9.6
533 splenic disease 9.6
534 epidermolysis bullosa 9.6
535 cervix carcinoma 9.6
536 substance abuse 9.6
537 gingival overgrowth 9.6
538 papillary carcinoma 9.6
539 thymoma 9.6
540 embryonal carcinoma 9.6
541 angiomyolipoma 9.6
542 gm1 gangliosidosis 9.6
543 fibrosarcoma 9.6
544 skin carcinoma 9.6
545 unverricht-lundborg syndrome 9.6
546 choriocarcinoma 9.6
547 skin disease 9.6
548 gastric adenocarcinoma 9.6
549 plasmacytoma 9.6
550 arthropathy 9.6
551 nodular basal cell carcinoma 9.6
552 neuromuscular disease 9.6
553 rhinitis 9.6
554 secretory meningioma 9.6
555 lymphoplasmacyte-rich meningioma 9.6
556 brain edema 9.6
557 cavernous hemangioma 9.6
558 thyroid gland disease 9.6
559 intestinal disease 9.6
560 epulis 9.6
561 pneumonia 9.6
562 lymphopenia 9.6
563 inflammatory breast carcinoma 9.6
564 connective tissue disease 9.6
565 hepatoblastoma 9.6
566 t-cell leukemia 9.6
567 end stage renal failure 9.6
568 cocaine abuse 9.6
569 chronic rhinitis 9.6
570 influenza 9.6
571 arthritis 9.6
572 monocytic leukemia 9.6
573 chickenpox 9.6
574 eating disorder 9.6
575 actinic keratosis 9.6
576 autosomal dominant polycystic kidney disease 9.6
577 leishmaniasis 9.6
578 cutaneous leishmaniasis 9.6
579 ocular hypertension 9.6
580 cleft lip 9.6
581 acute myocardial infarction 9.6
582 primary ciliary dyskinesia 9.6
583 congenital disorders of n-linked glycosylation and multiple pathway 9.6
584 genetic prion diseases 9.6
585 rab18 deficiency 9.6
586 actinic cheilitis 9.6
587 cor triatriatum 9.6
588 dwarfism 9.6
589 gangliosidosis 9.6
590 mycobacterium fortuitum 9.6
591 skeletal dysplasias 9.6
592 spastic paraplegia 12 9.6
593 viral hemorrhagic fever 9.6
594 x-linked charcot-marie-tooth disease 9.6
595 x-linked complicated spastic paraplegia type 1 9.6
596 age-related hearing loss 9.6
597 anoxia 9.6
598 febrile seizures 9.6
599 headache 9.6
600 inherited prion disease 9.6
601 erythrokeratoderma 9.6
602 overgrowth syndrome 9.6
603 spermatogenic failure 6 9.5
604 spondyloarthropathy 1 9.5
605 arteries, anomalies of 9.5
606 machado-joseph disease 9.5
607 cardiac arrhythmia 9.5
608 charcot-marie-tooth disease, demyelinating, type 1b 9.5
609 charcot-marie-tooth disease and deafness 9.5
610 cornea plana 1, autosomal dominant 9.5
611 creutzfeldt-jakob disease 9.5
612 cri-du-chat syndrome 9.5
613 optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy 9.5
614 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.5
615 elastosis perforans serpiginosa 9.5
616 erythroleukemia, familial 9.5
617 erythrokeratodermia variabilis et progressiva 1 9.5
618 esophageal cancer 9.5
619 gilles de la tourette syndrome 9.5
620 renal cysts and diabetes syndrome 9.5
621 hand skill, relative 9.5
622 hashimoto thyroiditis 9.5
623 spondyloepiphyseal dysplasia with congenital joint dislocations 9.5
624 multiple system atrophy 1 9.5
625 inclusion body myositis 9.5
626 keratitis, hereditary 9.5
627 laryngomalacia 9.5
628 lichen sclerosus et atrophicus 9.5
629 lipomatosis, multiple 9.5
630 macular dystrophy, vitelliform, 2 9.5
631 medulloblastoma 9.5
632 monilethrix 9.5
633 neurofibromatosis, type i 9.5
634 neurofibromatosis, type iv, of riccardi 9.5
635 nevus, epidermal 9.5
636 oculopharyngeal muscular dystrophy 9.5
637 optic atrophy 1 9.5
638 palatopharyngeal incompetence 9.5
639 pancreatitis, hereditary 9.5
640 isolated growth hormone deficiency, type ii 9.5
641 pneumothorax, primary spontaneous 9.5
642 prader-willi syndrome 9.5
643 pelvic organ prolapse 9.5
644 exfoliation syndrome 9.5
645 retinal detachment 9.5
646 schizophrenia 1 9.5
647 spastic paraplegia 4, autosomal dominant 9.5
648 steatocystoma multiplex 9.5
649 tobacco addiction 9.5
650 torus palatinus and torus mandibularis 9.5
651 wilms tumor 1 9.5
652 leber congenital amaurosis 1 9.5
653 central hypoventilation syndrome, congenital 9.5
654 buerger disease 9.5
655 tumoral calcinosis, hyperphosphatemic, familial, 1 9.5
656 chondrosarcoma 9.5
657 conotruncal heart malformations 9.5
658 friedreich ataxia 9.5
659 gaucher disease, type ii 9.5
660 hemangiopericytoma, malignant 9.5
661 muscular dystrophy-dystroglycanopathy , type a, 1 9.5
662 vici syndrome 9.5
663 immune deficiency disease 9.5
664 chylomicron retention disease 9.5
665 lipoid proteinosis of urbach and wiethe 9.5
666 familial mediterranean fever 9.5
667 spinal muscular atrophy, type ii 9.5
668 muscular dystrophy-dystroglycanopathy , type a, 4 9.5
669 myopathy, congenital 9.5
670 ceroid lipofuscinosis, neuronal, 1 9.5
671 nonarteritic anterior ischemic optic neuropathy 9.5
672 peters-plus syndrome 9.5
673 interstitial pneumonitis, desquamative, familial 9.5
674 progesterone resistance 9.5
675 pulmonary venoocclusive disease 1, autosomal dominant 9.5
676 robinow syndrome, autosomal recessive 1 9.5
677 senile plaque formation 9.5
678 multiple sulfatase deficiency 9.5
679 oliver-mcfarlane syndrome 9.5
680 chanarin-dorfman syndrome 9.5
681 usher syndrome, type i 9.5
682 congenital hemidysplasia with ichthyosiform erythroderma and limb defects 9.5
683 ifap syndrome with or without bresheck syndrome 9.5
684 mucopolysaccharidosis, type ii 9.5
685 premature ovarian failure 1 9.5
686 pelizaeus-merzbacher disease 9.5
687 spondyloepiphyseal dysplasia tarda, x-linked 9.5
688 retinitis pigmentosa-deafness syndrome 9.5
689 warburg micro syndrome 1 9.5
690 epilepsy, childhood absence 1 9.5
691 retinitis pigmentosa 11 9.5
692 adenomyosis 9.5
693 gallbladder disease 1 9.5
694 brody myopathy 9.5
695 hypocalcemia, autosomal dominant 1 9.5
696 stuve-wiedemann syndrome 9.5
697 ceroid lipofuscinosis, neuronal, 6 9.5
698 hyperinsulinemic hypoglycemia, familial, 2 9.5
699 autoimmune lymphoproliferative syndrome 9.5
700 cholestasis, progressive familial intrahepatic, 3 9.5
701 gracile syndrome 9.5
702 spastic paraplegia 8, autosomal dominant 9.5
703 orthostatic intolerance 9.5
704 paragangliomas 3 9.5
705 basal cell carcinoma 1 9.5
706 nonaka myopathy 9.5
707 maturity-onset diabetes of the young 9.5
708 maturity-onset diabetes of the young, type 4 9.5
709 muscular dystrophy-dystroglycanopathy , type b, 5 9.5
710 lymphangioleiomyomatosis 9.5
711 epiphyseal dysplasia, multiple, 5 9.5
712 aortic aneurysm, familial thoracic 1 9.5
713 spinocerebellar ataxia 17 9.5
714 allergic rhinitis 9.5
715 muscular dystrophy-dystroglycanopathy , type c, 5 9.5
716 caspase 8 deficiency 9.5
717 resting heart rate, variation in 9.5
718 vitamin k-dependent clotting factors, combined deficiency of, 2 9.5
719 mycobacterium tuberculosis 1 9.5
720 leukemia, chronic myeloid 9.5
721 hermansky-pudlak syndrome 2 9.5
722 sick sinus syndrome 1 9.5
723 hyperinsulinemic hypoglycemia, familial, 5 9.5
724 hyperinsulinemic hypoglycemia, familial, 4 9.5
725 corneal dystrophy, congenital stromal 9.5
726 asthma-related traits 4 9.5
727 malaria 9.5
728 smoking as a quantitative trait locus 3 9.5
729 colorectal cancer 5 9.5
730 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.5
731 parkinson disease 14, autosomal recessive 9.5
732 hypotrichosis and recurrent skin vesicles 9.5
733 mononeuropathy of the median nerve, mild 9.5
734 long qt syndrome 5 9.5
735 spermatogenic failure 9 9.5
736 barrett esophagus 9.5
737 tumor predisposition syndrome 9.5
738 graft-versus-host disease 9.5
739 accelerated tumor formation 9.5
740 membranous nephropathy 9.5
741 leptin deficiency or dysfunction 9.5
742 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 9.5
743 pulmonary hypertension, primary, 2 9.5
744 hyperprolactinemia 9.5
745 melioidosis 9.5
746 cholangiocarcinoma 9.5
747 bardet-biedl syndrome 4 9.5
748 autoimmune lymphoproliferative syndrome, type v 9.5
749 osteogenesis imperfecta, type xvi 9.5
750 spinocerebellar ataxia, autosomal recessive 20 9.5
751 autoimmune interstitial lung, joint, and kidney disease 9.5
752 corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia 9.5
753 hydrops, lactic acidosis, and sideroblastic anemia 9.5
754 nevus comedonicus 9.5
755 erythrokeratodermia variabilis et progressiva 5 9.5
756 alkuraya-kucinskas syndrome 9.5
757 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies 9.5
758 stargardt disease 9.5
759 autoimmune cardiomyopathy 9.5
760 keshan disease 9.5
761 acute diarrhea 9.5
762 cryptogenic organizing pneumonia 9.5
763 argentine hemorrhagic fever 9.5
764 restless legs syndrome 9.5
765 usher syndrome 9.5
766 exanthema subitum 9.5
767 exudative vitreoretinopathy 9.5
768 alcohol-related neurodevelopmental disorder 9.5
769 secondary progressive multiple sclerosis 9.5
770 peripheral artery disease 9.5
771 diabetic encephalopathy 9.5
772 oppositional defiant disorder 9.5
773 colorectal adenoma 9.5
774 colorectal adenocarcinoma 9.5
775 in situ pulmonary adenocarcinoma 9.5
776 ovarian clear cell carcinoma 9.5
777 endocervical adenocarcinoma 9.5
778 autosomal recessive cerebellar ataxia 9.5
779 pervasive developmental disorder 9.5
780 generalized epilepsy with febrile seizures plus 9.5
781 warburg micro syndrome 9.5
782 sclerosteosis 9.5
783 robinow syndrome 9.5
784 pollen allergy 9.5
785 hyperekplexia 9.5
786 isolated growth hormone deficiency 9.5
787 progressive familial intrahepatic cholestasis 9.5
788 bone disease 9.5
789 hepatic veno-occlusive disease 9.5
790 polycystic kidney disease 9.5
791 x-linked alport syndrome 9.5
792 endometritis 9.5
793 thymus lymphoma 9.5
794 pleomorphic lipoma 9.5
795 parotitis 9.5
796 sialadenitis 9.5
797 tonsillitis 9.5
798 rickets 9.5
799 protein-losing enteropathy 9.5
800 microphthalmia 9.5
801 gastric ulcer 9.5
802 microcephaly 9.5
803 hydrocephalus 9.5
804 borderline personality disorder 9.5
805 cholesteatoma of middle ear 9.5
806 lipoid nephrosis 9.5
807 spastic quadriplegia 9.5
808 alport syndrome 9.5
809 corneal edema 9.5
810 brucellosis 9.5
811 asphyxia neonatorum 9.5
812 rabies 9.5
813 pulmonary edema 9.5
814 pyelonephritis 9.5
815 diphtheria 9.5
816 hemopericardium 9.5
817 diabetic autonomic neuropathy 9.5
818 polycystic ovary syndrome 9.5
819 hyperandrogenism 9.5
820 dental pulp necrosis 9.5
821 lyme disease 9.5
822 pericardial effusion 9.5
823 coronary thrombosis 9.5
824 inflammatory spondylopathy 9.5
825 hemosiderosis 9.5
826 cartilage disease 9.5
827 primary biliary cirrhosis 9.5
828 crimean-congo hemorrhagic fever 9.5
829 atypical depressive disorder 9.5
830 granular corneal dystrophy 9.5
831 cough variant asthma 9.5
832 bronchopneumonia 9.5
833 vulva cancer 9.5
834 retinal ischemia 9.5
835 pseudobulbar palsy 9.5
836 locked-in syndrome 9.5
837 nephronophthisis 9.5
838 quadriplegia 9.5
839 keratoconjunctivitis sicca 9.5
840 sialolithiasis 9.5
841 hereditary spherocytosis 9.5
842 conduct disorder 9.5
843 crescentic glomerulonephritis 9.5
844 acute cystitis 9.5
845 gout 9.5
846 porphyria 9.5
847 ehlers-danlos syndrome 9.5
848 polyneuropathy 9.5
849 bird fancier's lung 9.5
850 facial paralysis 9.5
851 amenorrhea 9.5
852 gonadal dysgenesis 9.5
853 cystic echinococcosis 9.5
854 echinococcosis 9.5
855 disease of mental health 9.5
856 avoidant personality disorder 9.5
857 chronic cervicitis 9.5
858 angioedema 9.5
859 rheumatic fever 9.5
860 endogenous depression 9.5
861 intraductal papilloma 9.5
862 benign breast phyllodes tumor 9.5
863 ventricular septal defect 9.5
864 ichthyosis 9.5
865 thyroid gland cancer 9.5
866 calcinosis 9.5
867 bone cancer 9.5
868 viral hepatitis 9.5
869 bardet-biedl syndrome 9.5
870 adenosarcoma 9.5
871 rectum cancer 9.5
872 exostosis 9.5
873 hyperostosis 9.5
874 vaginitis 9.5
875 myeloproliferative neoplasm 9.5
876 focal epilepsy 9.5
877 pharyngitis 9.5
878 colon adenocarcinoma 9.5
879 arteriosclerosis 9.5
880 cervicitis 9.5
881 agammaglobulinemia 9.5
882 larynx cancer 9.5
883 capillary hemangioma 9.5
884 bilirubin metabolic disorder 9.5
885 tic disorder 9.5
886 contact dermatitis 9.5
887 acute interstitial pneumonia 9.5
888 membranoproliferative glomerulonephritis 9.5
889 newcastle disease 9.5
890 cystic kidney disease 9.5
891 lobular neoplasia 9.5
892 gingivitis 9.5
893 gallbladder cancer 9.5
894 keratoacanthoma 9.5
895 junctional epidermolysis bullosa 9.5
896 rhabdomyosarcoma 9.5
897 vaccinia 9.5
898 bone inflammation disease 9.5
899 mesenchymal cell neoplasm 9.5
900 liposarcoma 9.5
901 blepharochalasis 9.5
902 cellulitis 9.5
903 turner syndrome 9.5
904 aortic aneurysm 9.5
905 intermittent claudication 9.5
906 lung benign neoplasm 9.5
907 ovary adenocarcinoma 9.5
908 anovulation 9.5
909 hidradenoma 9.5
910 pancreatic adenocarcinoma 9.5
911 nail disease 9.5
912 systemic scleroderma 9.5
913 pyoderma 9.5
914 histiocytoma 9.5
915 coronary stenosis 9.5
916 superficial basal cell carcinoma 9.5
917 smooth muscle tumor 9.5
918 pustulosis of palm and sole 9.5
919 seminoma 9.5
920 bartter disease 9.5
921 granulomatous endometritis 9.5
922 holoprosencephaly 9.5
923 prostate disease 9.5
924 proliferative glomerulonephritis 9.5
925 movement disease 9.5
926 adenosquamous carcinoma 9.5
927 intrahepatic cholangiocarcinoma 9.5
928 adjustment disorder 9.5
929 middle ear disease 9.5
930 urinary tract obstruction 9.5
931 colonic disease 9.5
932 schizoaffective disorder 9.5
933 pulmonary venoocclusive disease 9.5
934 acute pyelonephritis 9.5
935 agoraphobia 9.5
936 acquired immunodeficiency syndrome 9.5
937 spondylitis 9.5
938 dentin sensitivity 9.5
939 thyroiditis 9.5
940 meningothelial meningioma 9.5
941 malignant pleural mesothelioma 9.5
942 peptic ulcer disease 9.5
943 macular holes 9.5
944 placenta disease 9.5
945 hyperthyroidism 9.5
946 periampullary adenocarcinoma 9.5
947 osteochondrosis 9.5
948 periapical periodontitis 9.5
949 appendicitis 9.5
950 osteochondritis dissecans 9.5
951 extrinsic allergic alveolitis 9.5
952 kidney angiomyolipoma 9.5
953 fundus dystrophy 9.5
954 bullous pemphigoid 9.5
955 pyoderma gangrenosum 9.5
956 subacute delirium 9.5
957 tongue cancer 9.5
958 decubitus ulcer 9.5
959 vascular dementia 9.5
960 megakaryocytic leukemia 9.5
961 rubella 9.5
962 molluscum contagiosum 9.5
963 rosacea 9.5
964 psoriasis 9.5
965 progressive myoclonus epilepsy 9.5
966 cowpox 9.5
967 cervix uteri carcinoma in situ 9.5
968 zellweger syndrome 9.5
969 hard palate cancer 9.5
970 amebiasis 9.5
971 pemphigus 9.5
972 lichen planus 9.5
973 urea cycle disorder 9.5
974 viral infectious disease 9.5
975 keratoconjunctivitis 9.5
976 intracranial hypertension 9.5
977 cholangitis 9.5
978 meningitis 9.5
979 dacryoadenitis 9.5
980 neurofibroma 9.5
981 kidney hypertrophy 9.5
982 aphthous stomatitis 9.5
983 pulmonary emphysema 9.5
984 toxic myocarditis 9.5
985 vitreous detachment 9.5
986 polyarteritis nodosa 9.5
987 dacryocystitis 9.5
988 toxoplasmosis 9.5
989 drug dependence 9.5
990 distal hereditary motor neuropathies 9.5
991 limb-girdle muscular dystrophy 9.5
992 bap1 tumor predisposition syndrome 9.5
993 berardinelli-seip congenital lipodystrophy 9.5
994 hereditary dystonia 9.5
995 huppke-brendel syndrome 9.5
996 ngly1-related congenital disorder of deglycosylation 9.5
997 nsdhl-related disorders 9.5
998 spastic paraplegia 4 9.5
999 spastic paraplegia 8 9.5
1000 trichorhinophalangeal syndrome 9.5
1001 wfs1-related disorders 9.5
1002 acute mountain sickness 9.5
1003 autoimmune myocarditis 9.5
1004 cardiac rupture 9.5
1005 cerebellar degeneration 9.5
1006 cervical intraepithelial neoplasia 9.5
1007 children's interstitial lung disease 9.5
1008 chronic graft versus host disease 9.5
1009 chronic thromboembolic pulmonary hypertension 9.5
1010 cluster headache 9.5
1011 congenital hemolytic anemia 9.5
1012 congenital muscular dystrophy due to dystroglycanopathy 9.5
1013 disseminated infection with mycobacterium avium complex 9.5
1014 early-onset, autosomal dominant alzheimer disease 9.5
1015 familial tumoral calcinosis 9.5
1016 growth hormone deficiency 9.5
1017 haemophilus influenzae 9.5
1018 hemorrhagic shock and encephalopathy syndrome 9.5
1019 homologous wasting disease 9.5
1020 ichthyosis follicularis atrichia photophobia syndrome 9.5
1021 laugier-hunziker syndrome 9.5
1022 muscle eye brain disease 9.5
1023 myoclonus epilepsy 9.5
1024 oral lichen planus 9.5
1025 orofacial granulomatosis 9.5
1026 painful legs and moving toes syndrome 9.5
1027 parainfluenza virus type 3 9.5
1028 ring chromosome 16 9.5
1029 soft tissue sarcoma 9.5
1030 splenomegaly 9.5
1031 sutton disease 2 9.5
1032 testicular seminoma 9.5
1033 tracheobronchomalacia 9.5
1034 trichofolliculoma 9.5
1035 fainting 9.5
1036 head injury 9.5
1037 hypotonia 9.5
1038 postherpetic neuralgia 9.5
1039 syncope 9.5
1040 cleft lip/palate 9.5
1041 cerebrofacial arteriovenous metameric syndrome 9.5
1042 obsolete: atypical teratoid/rhabdoid tumor 9.5
1043 serpinopathy 9.5
1044 genetic interstitial lung disease 9.5
1045 pulmonary hypertension owing to lung disease and/or hypoxia 9.5
1046 obsolete: rapidly progressive glomerulonephritis 9.5
1047 semilobar holoprosencephaly 9.5
1048 rare hereditary hemochromatosis 9.5
1049 papular elastorrhexis 9.5
1050 qualitative or quantitative defects of alpha-dystroglycan 9.5
1051 ciliopathy 9.5
1052 familial intrahepatic cholestasis 9.5
1053 idiopathic avascular necrosis 9.5
1054 malignant epithelial tumor of ovary 9.5
1055 extracranial carotid artery aneurysm 9.5
1056 congenital amyoplasia 9.5
1057 cebpe-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome 9.5
1058 inherited retinal disorder 9.5
1059 pik3ca-related overgrowth syndrome 9.5
1060 serotonin syndrome 9.5
1061 rare tumor 9.5
1062 rare surgical neurologic disease 9.5
1063 polyploidy 9.5
1064 uremic pruritus 9.5
1065 vitreoretinopathy 9.5
1066 stromal corneal dystrophy 9.5
1067 autosomal dominant pure spastic paraplegia 9.5
1068 thyroid tumor 9.5

Graphical network of the top 20 diseases related to Amelogenesis Imperfecta Hypoplastic Type, Ig:



Diseases related to Amelogenesis Imperfecta Hypoplastic Type, Ig

Symptoms & Phenotypes for Amelogenesis Imperfecta Hypoplastic Type, Ig

UMLS symptoms related to Amelogenesis Imperfecta Hypoplastic Type, Ig:


polyuria

Drugs & Therapeutics for Amelogenesis Imperfecta Hypoplastic Type, Ig

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Anatomical Context for Amelogenesis Imperfecta Hypoplastic Type, Ig

MalaCards organs/tissues related to Amelogenesis Imperfecta Hypoplastic Type, Ig:

40
Breast, Lung, Kidney, Bone, Thyroid, Heart, Liver

Publications for Amelogenesis Imperfecta Hypoplastic Type, Ig

Articles related to Amelogenesis Imperfecta Hypoplastic Type, Ig:

(showing 4, show less)
# Title Authors PMID Year
1
Enamel renal syndrome: a rare case report. 61
22918105 2012
2
Amelogenesis imperfecta, nephrocalcinosis, and hypocalciuria syndrome in two siblings from a large family with consanguineous parents. 61
9870488 1998
3
Ultrastructural study of tooth enamel with amelogenesis imperfecta in AI-nephrocalcinosis syndrome. 61
7554924 1995
4
Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolism. 61
3872071 1985

Variations for Amelogenesis Imperfecta Hypoplastic Type, Ig

Expression for Amelogenesis Imperfecta Hypoplastic Type, Ig

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GO Terms for Amelogenesis Imperfecta Hypoplastic Type, Ig

Sources for Amelogenesis Imperfecta Hypoplastic Type, Ig

3 CDC
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10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
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28 GO
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31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
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39 LOVD
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49 NCIt
50 NDF-RT
53 NINDS
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63 QIAGEN
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