Xenbase

Search Diseases

Alphabetic Search:

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

???pagination.result.count???

???pagination.result.page??? ???pagination.result.prev??? 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 ???pagination.result.next???

Disease	Synonyms	Description
Ambras type hypertrichosis universalis congenita	Ambras syndrome; HTC1	A hypertrichosis characterized by autosomal domina..[+] A hypertrichosis characterized by autosomal dominant inheritance of the presence of vellus-type hair on the entire body, especially on the face, ears and shoulders, with the exception of palms, soles, and mucous membranes that has_material_basis_in chromosomal abnormalities in the region 8q22. [-]
autosomal recessive distal hereditary motor neuronopathy 1	autosomal recessive distal spinal muscular atrophy.. [+] autosomal recessive distal spinal muscular atrophy 1; autosomal recessive spinal muscular atrophy with respiratory distress; dHMN6; diaphragmatic spinal muscular atrophy; distal hereditary motor neuropathy type 6; distal-HMN type 6; severe infantile axonal neuropathy with respiratory failure type 1; SIANRF; SMARD1; spinal muscular atrophy with respiratory distress type 1; DSMA1; distal spinal muscular atrophy 1 [-]	A spinal muscular atrophy characterized by autosom..[+] A spinal muscular atrophy characterized by autosomal recessive inheritance of severe respiratory distress resulting from diaphragmatic paralysis that predominantly involves the upper limbs and distal muscles that has_material_basis_in homozygous or compound heterozygous mutation in the IGHMBP2 gene on chromosome 11q13. [-]
autosomal recessive distal hereditary motor neuronopathy 2	autosomal recessive distal spinal muscular atrophy.. [+] autosomal recessive distal spinal muscular atrophy 2; DSMA2; spinal muscular atrophy Jerash type; dHMNJ; distal hereditary motor neuropathy Jerash type; distal spinal muscular atrophy 2 [-]	A spinal muscular atrophy characterized by autosom..[+] A spinal muscular atrophy characterized by autosomal recessive inheritance of distal muscle weakness and muscle wasting primarily affecting the upper and lower limbswith onset typically in the first decade of life that has_material_basis_in homozygous mutation in the SIGMAR1 gene on chromosome 9p13. [-]
acquired von Willebrand syndrome	AVWS	A blood coagulation disease characterized by devel..[+] A blood coagulation disease characterized by development of a defect in clotting in the absence of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age. Typically this develops secondarily to other disorders, such as lymphoproliferative, myeloproliferative, cardiovascular and autoimmune disorders. [-]
angioimmunoblastic T-cell lymphoma		A peripheral T-cell lymphoma characterized by auto..[+] A peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis. [-]
autosomal recessive isolated ectopia lentis 2	ECTOL2	An isolated ectopia lentis that has_material_basis..[+] An isolated ectopia lentis that has_material_basis_in homozygous or compound heterozygous mutation in the ADAMTSL4 gene on chromosome 1q21. [-]
autosomal dominant isolated ectopia lentis 1	ECTOL1	An isolated ectopia lentis that has_material_basis..[+] An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21. [-]
autosomal recessive spinocerebellar ataxia 21	autosomal recessive spinocerebellar ataxia 21 with.. [+] autosomal recessive spinocerebellar ataxia 21 with hepatopathy; acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome; SCAR21 [-]	An autosomal recessive cerebellar ataxia that has_..[+] An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13. [-]
autosomal dominant sensory ataxia 1	ADSA; SNAX1	A hereditary ataxia characterized by gait difficul..[+] A hereditary ataxia characterized by gait difficulty and instability especially in dark conditions resulting from sensory loss in the extremities and without cerebellar involvement that has_material_basis_in heterozygous mutations in the RNF170 gene on chromosome 8. [-]
autosomal dominant adult-onset proximal spinal muscular atrophy	autosomal dominant late-onset spinal muscular atro.. [+] autosomal dominant late-onset spinal muscular atrophy, Finkel type; autosomal dominant adult-onset proximal SMA; autosomal dominant adult proximal spinal muscular atrophy; Finkel disease; Finkel late-adult type SMA; SMAFK [-]	A spinal muscular atrophy characterized by adult-o..[+] A spinal muscular atrophy characterized by adult-onset of slowly progressive, proximal muscular weakness with fasciculations and absent/hypoactive deep tendon reflexes, without bulbar or pyramidal involvement that has_material_basis_in heterozygous mutation in VAPB on 20q13. [-]
autosomal recessive distal hereditary motor neuronopathy	autosomal recessive distal spinal muscular atrophy.. [+] autosomal recessive distal spinal muscular atrophy [-]	A spinal muscular atrophy that has_material_basis_..[+] A spinal muscular atrophy that has_material_basis_in autosomal recessive inheritance. [-]
autosomal dominant distal hereditary motor neuronopathy	autosomal dominant distal spinal muscular atrophy; .. [+] autosomal dominant distal spinal muscular atrophy; autosomal dominant distal hereditary motor neuropathy; autosomal dominant dHMN [-]	A spinal muscular atrophy that is characterized by..[+] A spinal muscular atrophy that is characterized by progressive distal motor weakness and muscular atrophy of the peripheral nervous system without sensory impairment, that is caused by anterior horn cell degeneration, and that has_material_basis_in autosomal dominant inheritance. [-]
autosomal dominant distal hereditary motor neuronopathy 7	dHMN7; DHMNVPy; distal spinal muscular atrophy wit.. [+] dHMN7; DHMNVPy; distal spinal muscular atrophy with vocal cord paralysis; DHMN7A; distal hereditary motor neuronopathy type 7; distal hereditary motor neuropathy type VIIA; distal spinal muscular atrophy with vocal cord paralysis type 7A; Harper-Young myopath; HMN VIIA; HMN7A [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that is characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis and that has_material_basis_in heterozygous mutation in the SLC5A7 gene on 2q12.3. [-]
autosomal dominant distal hereditary motor neuronopathy 1	autosomal dominant distal juvenile spinal muscular.. [+] autosomal dominant distal juvenile spinal muscular atrophy type 1; dHMN1; distal hereditary motor neuropathy type I; HMN I; spinal Charcot-Marie-Tooth disease 1; distal hereditary motor neuronopathy type 1 [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that is characterized by progressive distal motor weakness and muscular atrophy of the peripheral nervous system without sensory impairment, that is caused by anterior horn cell degeneration and that has_material_basis_in heterozygous 1.35-Mb DNA insertion on chromosome 7q34-q36.2. This structural variant (SV) results in the production of a novel gene-intergenic fusion transcript, UBE3C-IF. [-]
autosomal dominant distal hereditary motor neuronopathy 14	DHMN7B; distal hereditary motor neuronopathy type .. [+] DHMN7B; distal hereditary motor neuronopathy type 7B; distal hereditary motor neuropathy type VIIB; distal spinal muscular atrophy with vocal cord paralysis type 7B; Harper-Young myopathy; HMN VIIB; HMN7B [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the DCTN1 gene on 2p13.1. [-]
autosomal dominant distal hereditary motor neuronopathy 5	DHMN5; distal hereditary motor neuropathy type V; .. [+] DHMN5; distal hereditary motor neuropathy type V; distal HMN V; distal spinal muscular atrophy type V; distal spinal muscular atrophy with upper limb predominance; DSMAV; HMN5; distal hereditary motor neuronopathy type 5; distal hereditary motor neuronopathy type 5A; distal HMN VA; distal spinal muscular atrophy type VA [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of distal muscle weakness and atrophy predominantly affecting the upper limbs in the first few decades of life and that has_material_basis_in heterozygous mutation in the GARS gene on chromosome 7p14. [-]
autosomal dominant distal hereditary motor neuronopathy 12	distal hereditary motor neuronopathy type 5B; dist.. [+] distal hereditary motor neuronopathy type 5B; distal HMN VB; distal spinal muscular atrophy type VB [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the REEP1 gene on 2p11.2. [-]
autosomal dominant distal hereditary motor neuronopathy 2	autosomal dominant adult spinal muscular atrophy I.. [+] autosomal dominant adult spinal muscular atrophy IIA; HMN II; HMN2; distal hereditary motor neuropathy type II; distal hereditary motor neuronopathy type 2; distal hereditary motor neuronopathy type 2A; distal hereditary motor neuropathy type IIA; HMN IIA; HMN2A; spinal Charcot-Marie-Tooth disease IIA [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life. [-]
autosomal dominant distal hereditary motor neuronopathy 3	distal hereditary motor neuropathy type IIB; HMN I.. [+] distal hereditary motor neuropathy type IIB; HMN IIB; HMN2B; distal hereditary motor neuronopathy type 2B [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the gene encoding heat-shock 27-kD protein-1 (HSPB1) on chromosome 7q11.23. [-]
autosomal dominant distal hereditary motor neuronopathy 4	DHMN2C; distal hereditary motor neuronopathy type .. [+] DHMN2C; distal hereditary motor neuronopathy type 2C; distal hereditary motor neuropathy type IIC; HMN IIC; HMN2C [-]	A distal hereditary motor neuropathy that has_mate..[+] A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the HSPB3 gene on 5q11.2. [-]
autosomal dominant distal hereditary motor neuronopathy 6	distal hereditary motor neuronopathy type 2D; dist.. [+] distal hereditary motor neuronopathy type 2D; distal hereditary motor neuropathy type IID; distal spinal muscular atrophy with calf predominance; HMN IID; HMN2D [-]	A distal hereditary motor neuropathy that has_mate..[+] A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the FBXO38 gene on 5q32. [-]
autosomal recessive distal hereditary motor neuronopathy 3	autosomal recessive distal spinal muscular atrophy.. [+] autosomal recessive distal spinal muscular atrophy type 3; dHMN3 and dHMN4; distal hereditary motor neuropathy type 3 and type 4; dSMA3; distal spinal muscular atrophy type 3 [-]	An autosomal recessive distal hereditary motor neu..[+] An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and wasting with variable severity that has_material_basis_in homozygous mutation in a 2.6-cM region of chromosome 11q13.3. [-]
autosomal dominant distal hereditary motor neuronopathy 9	DHMN9; distal hereditary motor neuronopathy type 9.. [+] DHMN9; distal hereditary motor neuronopathy type 9; distal hereditary motor neuropathy type IX; HMN9 [-]	An autosomal domiant distal hereditary motor neuro..[+] An autosomal domiant distal hereditary motor neuronopathy that is characterized by juvenile onset of slowly progressive distal muscle weakness and atrophy affecting both the lower and upper limbs that has_material_basis_in heterozygous mutation in the WARS gene on 14q32.2. [-]
autosomal recessive distal hereditary motor neuronopathy 4	autosomal recessive lower motor neuron disease wit.. [+] autosomal recessive lower motor neuron disease with childhood onset; autosomal recessive distal spinal muscular atrophy type 4; DSMA4; distal spinal muscular atrophy type 4 [-]	An autosomal recessive distal hereditary motor neu..[+] An autosomal recessive distal hereditary motor neuronopathy characterized by onset in early childhood of rapidly progressing proximal muscle weakness with an early involvement of foot and hand muscles that has_material_basis_in homozygous or compound heterozygous mutation in PLEKHG5 on 1p36.31. [-]
autosomal recessive distal hereditary motor neuronopathy 5	autosomal recessive distal spinal muscular atrophy.. [+] autosomal recessive distal spinal muscular atrophy type 5; DSMA5; young adult-onset dHMN; young adult-onset distal hereditary motor neuropathy; distal spinal muscular atrophy type 5 [-]	An autosomal recessive distal hereditary motor neu..[+] An autosomal recessive distal hereditary motor neuronopathy characterized by young adult onset of slowly progressive distal muscle weakness and atrophy resulting in gait impairment and loss of reflexes that has_material_basis_in homozygous or compound heterozygous mutation in DNAJB2 on 2q35. [-]
autosomal dominant distal hereditary motor neuronopathy 8	autosomal dominant congenital benign spinal muscul.. [+] autosomal dominant congenital benign spinal muscular atrophy; autosomal dominant benign distal spinal muscular atrophy; congenital benign spinal muscular atrophy with contractures; congenital nonprogressive spinal muscular atrophy; DHMN8; distal hereditary motor neuronopathy type 8; distal hereditary motor neuropathy type VIII; HMN8 [-]	An autosomal dominant distal hereditary motor neur..[+] An autosomal dominant distal hereditary motor neuronopathy that is characterized by congenital, non-progressive, predominantly distal, lower limb muscle weakness and atrophy with variable serverity that has_material_basis_in heterozygous mutation in the TRPV4 gene on 12q24.11. [-]
autosomal recessive centronuclear myopathy	AR-CNM	A centronuclear myopathy that has_material_basis_i..[+] A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance. [-]
autosomal dominant centronuclear myopathy	AD-CNM	A centronuclear myopathy that has_material_basis_i..[+] A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance. [-]
acromicric dysplasia	ACMICD; acromicric skeletal dysplasia	An osteochondrodysplasia characterized by autosoma..[+] An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1. [-]
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1	ALS-PDC; amyotrophic lateral sclerosis-parkinsonis.. [+] ALS-PDC; amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam; Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome; Guam disease; parkinsonism-dementia-ALS complex; PDALS; Lytico-Bodig disease [-]	A neurodegenerative disease characterized by chron..[+] A neurodegenerative disease characterized by chronic, progressive amyotrophic lateral sclerosis and parkinsonism-dementia. Susceptibility to this disease is influenced by heterozygous mutation in TRPM7 on 15q21.2. [-]
autosomal recessive hyaline body myopathy	congenital myopathy 7B; MSMB; Myopathy, myosin sto.. [+] congenital myopathy 7B; MSMB; Myopathy, myosin storage, autosomal recessive [-]	A hyaline body myopathy that has_material_basis_in..[+] A hyaline body myopathy that has_material_basis_in compound heterozygous or homozygous mutation in MYH7 on 14q11.2. [-]
autosomal dominant hyaline body myopathy	congenital myopathy 7A; MSMA; myopathy with lysis .. [+] congenital myopathy 7A; MSMA; myopathy with lysis of type I myofibrils; Myopathy, myosin storage, autosomal dominant [-]	A hyaline body myopathy that has_material_basis_in..[+] A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2. [-]
adermatoglyphia	Absence of fingerprints; ADERM; ADG; Congenital ab.. [+] ADG; ADERM; Absence of fingerprints; Congenital absence of fingerprints; Immigration delay disease; Isolated congenital adermatoglyphia [-]	A skin disease characterized by lack of epidermal ..[+] A skin disease characterized by lack of epidermal ridges on the fingers, toes, palms and soles that has_material_basis_in heterozygous mutation in the SMARCAD1 gene on chromosome 4q22.3. [-]
Alzheimer's disease 9	Alzheimer's disease 9, late onset; AD9	An Alzheimer's disease that has_material_basis_in ..[+] An Alzheimer's disease that has_material_basis_in heterozygous mutation in the ABCA7 gene on chromosome 19p13.3. [-]
apolipoprotein C-III deficiency	HALP2; hyperalphalipoproteinemia 2	A cholesterol-ester transfer protein deficiency ch..[+] A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in the APOC3 gene on chromosome 11q23.3. [-]
autosomal dominant keratitis	hereditary keratitis	A keratitis characterized by corneal opacification..[+] A keratitis characterized by corneal opacification and vascularization and foveal hypoplasia that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13. [-]
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2	autosomal recessive progressive external ophthalmo.. [+] autosomal recessive progressive external ophthalmoplegia 2; adult-onset CPEO with mitochondrial myopathy; adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy; PEOB2 [-]	A chronic progressive external ophthalmoplegia cha..[+] A chronic progressive external ophthalmoplegia characterized by adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, and signs and symptoms of spinocerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the RNASEH1 gene on chromosome 2p25.3. [-]
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4	autosomal recessive progressive external ophthalmo.. [+] autosomal recessive progressive external ophthalmoplegia 4; adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency; adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency; PEOB4 [-]	A chronic progressive external ophthalmoplegia cha..[+] A chronic progressive external ophthalmoplegia characterized by adult onset of eye muscle weakness and proximal limb muscle weakness that has_material_basis_in homozygous or compound heterozygous mutation in the DGUOK gene on chromosome 2p13.1. [-]
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2	autosomal dominant progressive external ophthalmop.. [+] autosomal dominant progressive external ophthalmoplegia 2; PEOA2 [-]	A chronic progressive external ophthalmoplegia tha..[+] A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the SLC25A4 gene on chromosome 4q35.1. [-]
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5	autosomal dominant progressive external ophthalmop.. [+] autosomal dominant progressive external ophthalmoplegia 5; PEOA5 [-]	A chronic progressive external ophthalmoplegia tha..[+] A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the RRM2B gene on chromosome 8q22.3. [-]
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6	autosomal dominant progressive external ophthalmop.. [+] autosomal dominant progressive external ophthalmoplegia 6; DNA2-related mitochondrial DNA deletion syndrome; mitochondrial DNA deletion syndrome with limb-girdle weakness; mitochondrial DNA deletion syndrome with progressive myopathy; mtDNA deletion syndrome with limb-girdle weakness; mtDNA deletion syndrome with progressive myopathy; PEOA6 [-]	A chronic progressive external ophthalmoplegia cha..[+] A chronic progressive external ophthalmoplegia characterized by muscle weakness, mainly affecting the lower limbs, external ophthalmoplegia, exercise intolerance and mtDNA deletions that has_material_basis_in heterozygous mutation in the DNA2 gene on chromosome 10q21.3. [-]
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3	autosomal dominant progressive external ophthalmop.. [+] autosomal dominant progressive external ophthalmoplegia 3; PEOA3 [-]	A chronic progressive external ophthalmoplegia tha..[+] A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the TWNK gene on chromosome 10q24.31. [-]
autosomal dominant progressive external ophthalmoplegia 1	PEOA1	A chronic progressive external ophthalmoplegia tha..[+] A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the POLG gene on chromosome 15q26.1. [-]
autosomal recessive progressive external ophthalmoplegia 1	PEOB1	A chronic progressive external ophthalmoplegia tha..[+] A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the POLG gene on chromosome 15q26.1. [-]
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5	autosomal recessive progressive external ophthalmo.. [+] autosomal recessive progressive external ophthalmoplegia 5; PEOB5 [-]	A chronic progressive external ophthalmoplegia tha..[+] A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the TOP3A gene on chromosome 17p11.2. [-]
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4	autosomal dominant progressive external ophthalmop.. [+] autosomal dominant progressive external ophthalmoplegia 4; PEOA4 [-]	A chronic progressive external ophthalmoplegia tha..[+] A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the POLG2 gene on chromosome 17q23.3. [-]
aplasia of lacrimal and salivary glands	ALSG; congenital absence of lacrimal puncta and sa.. [+] ALSG; congenital absence of lacrimal puncta and salivary glands [-]	A syndrome characterized by irritable eyes, epipho..[+] A syndrome characterized by irritable eyes, epiphora, xerostomia, variable aplasia or hypoplasia of the lacrimal, parotid, submandibular, and sublingual glands, and absence of the lacrimal puncta that has_material_basis_in heterozygous mutation in the FGF10 gene on chromosome 5p12. [-]
Alkuraya-Kucinskas syndrome	ALKKUCS	A syndrome characterized by arthrogryposis, cerebr..[+] A syndrome characterized by arthrogryposis, cerebral parenchymal underdevelopment, clubfoot, and global developmental delay with severe cases being incompatible with life that has_material_basis_in homozygous or compound heterozygous mutation in the KIAA1109 gene on chromosome 4q27. [-]
autosomal dominant vitreoretinochoroidopathy	ADVIRC; vitreoretinochoroidopathy dominant; vitreo.. [+] ADVIRC; vitreoretinochoroidopathy dominant; vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos; VRCP autosomal dominant; vitreoretinochoroidopathy with microcornea, glaucoma, and cataract [-]	A hereditary retinal dystrophy characterized by ab..[+] A hereditary retinal dystrophy characterized by abnormal chorioretinal hypopigmentation and hyperpigmentation typically lying between the vortex veins and the ora serrata for 360 degrees and other ocular developmental anomalies that has_material_basis_in heterozygous mutation in the BEST1 gene on chromosome 11q12.3. [-]
autosomal dominant woolly hair	ADWH	A familial woolly hair syndrome that has_material_..[+] A familial woolly hair syndrome that has_material_basis_in heterozygous mutation in the KRT74 gene on chromosome 12q13.13. [-]

???pagination.result.page??? ???pagination.result.prev??? 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 ???pagination.result.next???