Atopic Dermatitis

About the Disease
Dermatitis, Atopic, also known as atopic dermatitis, is related to allergic disease and dermatitis, atopic, 3, and has symptoms including exanthema and pruritus. An important gene associated with Dermatitis, Atopic is FLG (Filaggrin), and among its related pathways/superpathways are MIF Mediated Glucocorticoid Regulation and Cytokine Signaling in Immune system. The drugs Zinc oxide and Coal tar have been mentioned in the context of this disorder. Affiliated tissues include skin, t cells and breast, and related phenotypes are cataract and ichthyosis

Common Targets
MRPS21 | LCE1B | CXCR5 | HIF1A | AMP-activated protein kinase (AMPK) | IL33 | G595 | IL22 | BDNF | TEC | D2HGDH | TACR3 | TGFB1 | TNFRSF6B | CCR10 | FFAR4 | WFIKKN2 | IL1RN | BEND4 | KCNV2 | Interleukin 17 (nonspecified subtype) | LCE1E | KLK7 | GPBAR1 | COL6A5 | LOC101927770 | ZBTB38 | GPR35 | CD247 | PADI4 | IL36RN | MAMDC4 | VWA5A | DUSP3 | LCE3B | G7099 | ERP27 | TLR10 | SPINK5 | IL13RA1 | TACR2 | Carnitine O-Palmitoyltransferase 1 (CPT-1) (nonspecified subtype) | F2RL1 | IGF2R | KCNA3 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | ELANE | P2RX1 | IL23A | SERPINB3 | LCE3C | GTSE1 | OPRK1 | PRECSIT | Melanin | OVOL1 | CDK4 | PTGR2 | ACAN | PDE4B | IL2RA | OPRM1 | SLC25A11 | Protein kinase C (nonspecified subtype) | CCR6 | IKBKB | MST1P2 | NR1H2 | PBLD | S100A7L2 | FKBP1A | CNR2 | Interleukin-1 (nonspecified subtype) | UAP1 | LGALS3 | EVI5 | CYSLTR1 | DAAM2 | CTNNA3 | AQP9 | KLK5 | ORAI1 | G7295 | ZNF652 | IL17RA | PPARA | TRAF3 | TYK2 | FLG | ERAP2 | AKR1C2 | STAT6 | F11R | IFNGR1 | CD1A | HLA-B | ROCK1 | IL-31 Receptor | SELL | FCGRT | IDH1 | SPRR2B | TRPV4 | NPSR1 | KPRP | PDGFRB | PGS1 | CD200R1L | AQP4 | LCK | ZFYVE26 | Alpha-2 Adrenergic receptors (nonspecified subtype) | TEX30 | BRD2 | TYR | mTOR complex 1 | ALOX12 | BMX | SLCO2B1 | C-X-C Chemokine Receptor CXCR1/CXCR2 (IL-8 Receptor) (nonspecified subtype) | Phospholipase A2 (nonspecified subtype) | ERBB3 | Lipoxygenase (nonspecified subtype) | SIGLEC8 | IL4R | G6352 | TRPC5 | GABRB2 | MYO10 | BRD4 | GABRG2 | HRH2 | CCR4 | AQP3 | Matrix Metalloproteinase (MMP) (nonspecified subtype) | TSPAN4 | CA6 | PIK3CD | SKIC3 | HLA-DRB1 | IGHE | Chymotrypsin (nonspecified subtype) | EGR1 | TRPM8 | HTR1A | DMTN | PCDH1 | CARD11 | MFHAS1 | ASAH1 | OCLN | TNFRSF18 | PPP3R2 | CYP1A1 | EHMT1 | SLC22A12 | POM121L2 | PCMTD1 | MOCS1 | G2475 | ANKRD36 | Protein Tyrosine Phosphatase (PTP) (nonspecified subtype) | ICAM1 | SLC6A2 | ACAD10 | MRPS23 | CLDN20 | URB1 | CNR1 | CARD14 | SPPL2A | PPP3CC | IL7R | TMED5 | PPARG | CLASP2 | P2RX3 | COASY | IL12RB1 | ADAM17 | TJP1 | SRCIN1 | PPID | BTNL2 | IQGAP1 | IL1RL1 | LOC105369325 | Glutamate Transporter (nonspecified subtype) | S1PR4 | HTR2B | ROS1 | DYRK1A | IL-2 receptor | ABCA1 | SSH1 | GSDMA | CXCR1 | HSD11B1 | MED12L | TRPV2 | IL17C | GABA(A) receptor | KRT6A | PTGS1 | IL-17 A/F heterodimer | Oxysterols receptor LXR (nonspecified subtype) | HDC | MIR2115 | EMSY | TIRAP | Tyrosine Kinase (nonspecified subtype) | alpha-Secretase (nonspecified subtype) | NTRK3 | CROCC | Gap junction Connexin ( (nonspecified subtype) | IL-4 receptor | OR2T27 | KDM3B | CCR2 | TRPV1 | PHLDB1 | USP14 | HLA-A | PFKFB3 | G3605 | G7124 | UCHL5 | GRM7 | HTATIP2 | HPGD | IL15 | SYK | ARID5B | FLT1 | SELP | OR1D5 | GSTT1 | PTPN1 | IL-20 receptor | PDPK1 | CYP24A1 | OR8B3 | ACHE | NTRK1 | DCHS1 | ITK | USP6 | Neurotrophic Tyrosine Kinase Receptor (TRK) (nonspecified subtype) | KRTAP5-8 | S100A5 | SPATA18 | NEDD4 | IRAK4 | Voltage-Gated Sodium Channel Complex | UBQLNL | AKR1B1 | S1PR3 | ENKUR | ADAMTSL1 | STAT5 (nonspecified subtype) | XDH | TMEM120A | NR3C1 | G3630 | Interleukin-12 (IL-12) | ACO2 | CDK6/Cyclin D1 | HRNR | TSLP | CCL11 | UBASH3A | ENTPD3 | MMP7 | TLR2 | MAP3K19 | PRKCH | CUL7 | G836 | RAD50 | Mitogen-Activated Protein Kinase (nonspecified subtype) | SSTR4 | MAP4K1 | Interferon (nonspecified subtype) | KRTAP1-3 | 15-Lipoxygenase (nonspecified subtype) | OPRD1 | CYP4F8 | NRP1 | ZDHHC8 | PTGDR | NPY4R | PTPN14 | G367 | IgE Receptors (nonspecified subtype) | UBR2 | LRRC8C | UHRF1 | GSDMB | H1-2 | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | LELP1 | G5743 | TRPC6 | G5747 | G4233 | QPCT | NR1H4 | mTOR complex 2 | FLG2 | TLE1 | EVPL | BLTP1 | CXCR3 | BCL2A1 | GABRA1 | TCN2 | TEK | RTEL1 | Sodium channel (nonspecified subtype) | VNN1 | Retinoid acid receptor (nonspecified subtype) | Ceramidase (nonspecified subtype) | IL5 | LRP1 | AKR1C3 | PTGDR2 | Toll-Like Receptor (nonspecified subtype) | ARSD | KLK2 | VDR | CHUK | Dual specificity protein kinase (CLK) (nonspecified subtype) | TRPV3 | IL17F | FLT3 | TNFRSF11A | NDE1 | Prostanoid TP receptor (nonspecified subtype) | CALCRL | Immunoglobulin E (IgE) | ALDH1L2 | CD200R1 | PDE6D | PDE4C | CCR9 | TREM1 | IL1A | CHIA | Kallikrein (nonspecified subtype) | CSF2 | Integrin alphaLbeta2 (LFA-1) receptor | TCHHL1 | IL2 | CDRT15 | KDR | MMP2 | MMP13 | LRRC8A | SLC6A4 | CCL17 | G196 | Sterol O-acyltransferase (ACAT) (nonspecified subtype) | RPTN | IL10 | IL25 | HSD11B2 | RET | ZNF365 | BRD3 | SLC16A5 | Janus Kinase (nonspecified subtype) | CHI3L1 | Tryptase (nonspecified subtype) | IL31 | OXER1 | CLEC16A | TBX6 | G1956 | CLDN1 | FPR2 | G5970 | PDGFRA | IL5RA | CXCR2 | ERBB4 | S1PR5 | TLR9 | PARP14 | LANCL2 | IL12A | NPSR1-AS1 | IFNG | ERAP1 | ROCK2 | SPHK1 | DYNLT4 | Cannabinoid receptor (nonspecified subtype) | OXR1 | PRR5L | IL1RL2 | HRH1 | TNFRSF4 | Inosine 5'-monophosphate dehydrogenase (IMPDH) (nonspecified subtype) | TRPA1 | High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7 (nonspecified protein) | TPSB2 | MBP | TACR1 | BLTP3A | PPP3CB | AHNAK2 | NLRP1 | NAMPT | APP | GLB1 | CYSLTR2 | CLDN4 | PDE4A | PRKCQ | IL31RA | CREBBP | CYP27A1 | PLA2G2D | GSTM1 | GSTP1 | CORIN | CCR5 | PPP3R1 | ALB | DOCK8 | SMAD3 | HLA-DPB1 | CRLF2 | C5AR1 | OSMR | Phospholipase A2, Secretory (sPLA2) (nonspecified subtype) | Chemokine receptor (nonspecified subtype) | Histamine Receptor (HR) (nonspecified subtype) | PPP2R3C | ACSM4 | LRP1B | Gap Junction Protein (nonspecified subtype) | CASP1 | Sterol Regulatory Element-Binding Protein (nonspecified subtype) | MIF | LRRC32 | IL22RA2 | LAMA3 | ZNF587 | DOK2 | CCL22 | GATA3 | KIF3A | NAAA | Retinoid RXR receptor (nonspecified subtype) | SPDEF | SH2D2A | IL6R | DEFB1 | IL20 | NLRP3 Inflammasome | CCL2 | TLR6 | HCAR2 | TENM4 | FLG-AS1 | IL1B | KIF18A | MRGPRX2 | IL4 | CRBN | G238 | KRR1 | JAK3 | ALOX5 | G3569 | IL-13 receptor | SLC9A4 | JAK1 | NLRX1 | PTGR3 | cGMP-inhibited 3',5'-cyclic phosphodiesterase 3 (PDE3) (nonspecified subtype) | TSBP1 | RNF123 | CTNNB1 | KCNJ10 | PLIN4 | IL36G | Mitogen-activated protein kinase (JNK) (nonspecified subtype) | MICA | G114548 | EGFLAM | HPGDS | HLA-C | JAK2 | CX3CR1 | CYP27B1 | PDE1A | RIPK1 | S1PR1 | FCER1A | DUOX1 | IL13 | MRGPRX4 | PSAPL1 | DDX55 | PIK3CG | GPR55 | G3576 | ITSN1 | TLR7 | NCOA1 | IL18 | PSG6 | CDK7 | HRH4 | GPSM3 | TXK | DOP1B | IL22RA1 | ZPBP2 | IL23R | DOP1A | CFLAR | SNORC | HLA-DQB1 | IL9R | NTRK2 | DENND4C | Interleukin 23 complex (IL-23) | UBR1 | CHCHD5 | Interleukin-7 receptor | AOC3 | ZNF354C | AURKA | PTAFR | PDE7A | LRRC43 | HSD17B3 | CMA1 | ELAC2 | NOP2 | ZNF662 | TLR1 | TRPM3 | Superoxide dismutase (SOD) (nonspecified subtype) | Defensin (nonspecified subtype) | INPP5D | TOGARAM1 | RNF170 | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | G6774 | LILRA6 | ALOX15 | G6647 | SLC25A34 | G5133 | CLDN23 | Monoamine oxidase (MAO) (nonspecified subtype) | NF-kappaB (NFkB) | TNFSF4 | PDE4D | SELE | METTL1 | KLK14 | CARD8 | G3620 | KIT | PLA2G2A | HDAC6 | IL12B | Sphingosine kinase (nonspecified subtype) | CDK4/Cyclin D1 | Protein Phosphatase 2B | RORC | TLR8 | ADAM10 | MC1R | NPY4R2 | PPIA | CCR3 | BTK | HRH3

Note: If you'd like to get a target analysis report for Atopic Dermatitis, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Atopic Dermatitis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Sitosterolemia | Wolff-Parkinson-White Syndrome | Endometritis | Myoclonus | Dyslexia | Colitis, Microscopic | Rift Valley Fever | Neonatal Progeroid Syndrome | Multifocal Motor Neuropathy | Chronic Thromboembolic Pulmonary Hypertension | Mumps | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Chondrodysplasia Punctata 2, X-linked Dominant | Meningitis | Wiskott-Aldrich Syndrome | Porphyria, Acute Intermittent | Kidney Stones | Myelomeningocele | Astrocytoma | Gigantism | Blepharophimosis Syndrome | Congenital Myasthenic Syndrome | Adenoma, Pleomorphic | Influenza | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | IgA Nephropathy | Cartilage Disorders | Epidermolysis Bullosa Acquisita | Osteoporosis | HIBCH Deficiency | Pemphigoid | Lymphoma, Mantle Cell | Myocardial Infarction | Albinism | Tularemia | Fascioliasis | Yellow Fever | Leishmaniasis, Visceral | Ellis-Van Creveld Syndrome | Hypertension, Essential | Non-small Cell Lung Cancer | Congenital Sodium Diarrhea | Lymphoma, B-cell | Vici Syndrome | Pneumothorax | Sarcoma, Ewing | Deafness, Dystonia, And Cerebral Hypomyelination | Hereditary Sensory Neuropathy Type 1 | Inborn Errors Of Metabolism | Prolactinoma | Japanese Encephalitis | Idiopathic Multicentric Castleman Disease | Cerebellar Ataxia, Cayman Type | Crisponi Syndrome | Gnathodiaphyseal Dysplasia | Cancer, Brain | Niemann-Pick Disease, Type B | Dementia, Vascular | Van Der Knaap Disease | Costello Syndrome | Medulloblastoma | Myeloid Leukemia | Presbyopia | Psoriasis | Ureteropelvic Junction Obstruction | COACH Syndrome | Xeroderma Pigmentosum Variant Type | Pyloric Stenosis, Infantile Hypertrophic | Rhabdoid Tumor | Leiomyosarcoma | SAPHO Syndrome | Glycogen Storage Disease Type 0, Muscle | Otitis Externa | Neurogenic Bladder | Liver Failure | Demyelinating Diseases | Hyperferritinemia-cataract Syndrome | Optic Nerve Hypoplasia, Bilateral | Early Infantile Epileptic Encephalopathy 13 | Polymyositis | Nanophthalmos | Crouzon Syndrome With Acanthosis Nigricans | Patent Ductus Arteriosus | Dysgerminoma | Retinal Vasculitis | IgA Deficiency | Colon Adenoma | Moyamoya Disease | Basal Ganglia Disease | Cardiomyopathy, Peripartum | Seizures | Charcot-Marie-Tooth Disease, Type 2A | Blue Rubber Bleb Nevus Syndrome | Chronic Myelomonocytic Leukemia | 3C Syndrome | Pemphigus | Milk Allergy | Infantile Spasm | Stickler Syndrome | Pseudohypoparathyroidism Type 1C | Hepatitis B, Chronic | Lipid Storage Myopathy | Mucolipidosis Type IV | Esophagitis | Schizoaffective Disorder | Polyradiculopathy | Cholesteryl Ester Storage Disease | Chromosome 5q Deletion Syndrome | Genitopatellar Syndrome | Schamberg Disease | Borjeson-Forssman-Lehmann Syndrome | Reticular Dysgenesis | Wolman Disease | Metaphyseal Chondrodysplasia, Schmid Type | Juvenile Myoclonic Epilepsy | Inflammatory Linear Verrucous Epidermal Nevus | Hypogonadism | Pterygium | Congenital Afibrinogenemia | Anthrax | KBG Syndrome | Macrodactyly | Epithelial-myoepithelial Carcinoma | Cramp Fasciculation Syndrome | Acute Leukemia | Raynaud Phenomenon | Leprosy | Alpha-thalassemia Myelodysplasia Syndrome | Hemophilia | Blood Protein Disorders | Diabetes Insipidus | Ameloblastoma | Progressive External Ophthalmoplegia | Myelitis | Tenosynovial Giant Cell Tumor | Diffuse Intrinsic Pontine Glioma | Porokeratosis | Learning Disability | Optic Neuropathy | Pseudohypoparathyroidism Type 2 | Waldenstrom Macroglobulinemia | Beta-Propeller Protein-associated Neurodegeneration | Narcolepsy | Macular Corneal Dystrophy Type 1 | Arthritis, Reactive | Angiomyolipoma | Colitis, Lymphocytic | LMNA-related Congenital Muscular Dystrophy | C3 Glomerulopathy | DiGeorge Syndrome | Primary Ovarian Insufficiency | Purpura, Thrombotic Thrombocytopenic | Stuttering | Frontometaphyseal Dysplasia | Cutaneous Mastocytosis | Steel Syndrome | Glutaric Aciduria Type 3 | Metanephric Adenoma | Familial Pheochromocytoma-paraganglioma | Hyperinsulinemic Hypoglycemia | Thyroid Dysgenesis | Nephrotic Syndrome | Carcinoid Syndrome | Sclerosing Cholangitis | Triphalangeal Thumb-polysyndactyly Syndrome | Pleurisy | Congenital Stationary Night Blindness | Lentigo | Glucagonoma | Monilethrix | Hyperkalemic Periodic Paralysis | Chorioretinitis | Hypertension, Portal | Prolidase Deficiency | Cystinuria | Postpartum Depression | Scabies | Von Willebrand Disease | Filariasis | Anti-NMDA Receptor Encephalitis | Rotor Syndrome | Pseudoexfoliation Syndrome | Ovarian Sex Cord-stromal Tumor | Spinocerebellar Ataxia Type 28 | Hepatitis, Chronic | Gangliosidosis, GM1 | Familial Episodic Pain Syndrome | Guttate Psoriasis | Hyperoxaluria | Endophthalmitis | Diabetic Encephalopathy | Chondrodysplasia Punctata | TARP Syndrome | Angiosarcoma Of The Breast | Liver Failure, Acute Infantile | DICER1 Syndrome | Hereditary Pyropoikilocytosis | Blepharo-cheilo-odontic Syndrome | Pupil Disorders | Myofibrillar Myopathy | Intracerebral Hemorrhage | Infertility | Cardiac Sarcoidosis | Benign Familial Infantile Seizures | Sotos Syndrome | Cholera | Achromatopsia | Ataxia-ocular Apraxia 2 | Botulism | Renal Tubular Dysgenesis | Pendred Syndrome | Long QT Syndrome Type 1 | Pyruvate Decarboxylase Deficiency | Pachyonychia Congenita | Huntington's Disease | Anodontia | Atrial Septal Defect | Poretti-Boltshauser Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Currarino Syndrome | Majeed Syndrome | Osteopetrosis | Cutaneous Lupus Erythematosus | Pancreatitis | Renal Hypomagnesemia 3 | Chorea-acanthocytosis | Phenylketonuria | Cellulitis | Isobutyryl-CoA Dehydrogenase Deficiency | Glycogen Storage Disease Type 6 | Hyperparathyroidism | Hemochromatosis | Binge Eating Disorder | Cervicitis | Lichen Planus | Vulvovaginitis | Benign Familial Neonatal Convulsions | Anuria | Chloridorrhea, Congenital | Paroxysmal Nocturnal Hemoglobinuria | Seborrheic Dermatitis | Gyrate Atrophy Of The Choroid And Retina | Auriculocondylar Syndrome | Epidermolysis Bullosa Dystrophica | Von Hippel-Lindau Disease | Paget's Disease Of The Breast | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Schwartz-Jampel-Aberfeld Syndrome | Antley-Bixler Syndrome | Syphilis | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Cohen Syndrome | Kabuki Syndrome | Dyskeratosis Congenita | McCune-Albright Syndrome | Genee-Wiedemann Syndrome | Methemoglobinemia Type IV | Hypercalcemia | Megaloblastic Anemia | Pantothenate Kinase-associated Neurodegeneration | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Periventricular Leukomalacia | Thrombotic Microangiopathy | Pleomorphic Xanthoastrocytoma | Acne Vulgaris | Fowler's Syndrome | Cyst | Lymphangioleiomyomatosis | Pneumonia, Mycoplasma | Adams-Oliver Syndrome | Schindler Disease | Hartsfield Syndrome | Aicardi-Goutieres Syndrome | Ovarian Hyperstimulation Syndrome | Tinea | Pierson Syndrome | Hyperammonemia | Granuloma Annulare | Autoimmune Hemolytic Anemia | Mastitis | Pulmonary Alveolar Proteinosis | Insulin Resistance | Crohn's Disease | Meningococcal Meningitis | Barakat Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Restless Legs Syndrome | Osteochondroma | Uremia | Meniere's Disease | Purpura | Ischemia | Crigler-Najjar Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Hepatopulmonary Syndrome | Usher Syndrome | Panniculitis | Hydrocephalus, Normal Pressure | Prostatitis | Fatty Aldehyde Dehydrogenase Deficiency | Sleep Apnea, Obstructive | Cryptococcal Meningitis | Meningioma | Anorchia | Veno-occlusive Disease | Nager Acrofacial Dysostosis | Renal Medullary Carcinoma | Hydrocephalus | Sengers Syndrome | Sarcoma | Ganglioglioma | Neurofibromatosis-Noonan Syndrome | Hypersensitivity Pneumonitis | Heimler Syndrome | Charcot-Marie-Tooth Disease Type 4B1 | Synpolydactyly | Knobloch Syndrome | Esophagitis, Eosinophilic | Pulmonary Alveolar Microlithiasis | Adenoma, Villous | Acromegaly | Microphthalmia, Syndromic 7 | Phenylketonuria II | Low Phospholipid Associated Cholelithiasis | Cardiomyopathy, Hypertrophic | Progressive Myoclonic Epilepsy | Facioscapulohumeral Muscular Dystrophy | Barrett Esophagus | Renal-hepatic-pancreatic Dysplasia | Cabezas Syndrome | Nail Disorder, Nonsyndromic Congenital | Bacterial Meningitis | Mitochondrial Encephalomyopathy | Lymphangioma | Gastric Atrophy | Thin Basement Membrane Disease | Urea Cycle Disorder | Dentinogenesis Imperfecta | Trachoma | Hyperbilirubinemia, Neonatal | Amebiasis | Distal Myopathy | Gynecomastia | Familial Hyperaldosteronism | Hyperphenylalaninemia | Joubert Syndrome 2 | Alopecia Areata | Chronic Beryllium Disease | Chordoma | Congenital Heart Block | Danon Disease | Asplenia | Atherosclerosis | Lipoma | Exostoses | Cockayne Syndrome | Gallstones | Cystinosis | Spinocerebellar Ataxia Type 6 | Venous Insufficiency | Prediabetes | Cystitis, Interstitial | Microcephalic Primordial Dwarfism | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Neurofibroma | Noonan Syndrome-like Disorder With Loose Anagen Hair | Strabismus | Carey-Fineman-Ziter Syndrome | HUPRA Syndrome | Primary Torsion Dystonia | Prader-Willi Syndrome | Wagner Disease | Bronchitis, Chronic | Diabetic Nephropathy | Glomerulonephritis | Hyperparathyroidism-jaw Tumor Syndrome | Spondylocarpotarsal Synostosis Syndrome | Speech Disorders | Chondromyxoid Fibroma | Urolithiasis | Ocular Albinism Type 1 | Polydactyly | Nestor-Guillermo Progeria Syndrome | Trichuriasis | Recurrent Respiratory Papillomatosis | Polycythemia | Fibronectin Glomerulopathy | Creatine Deficiency Syndrome Due To AGAT Deficiency | Canavan Disease | Low Tension Glaucoma | Klippel-Feil Syndrome | Chromosome 8q21.11 Deletion Syndrome | Brooke-Spiegler Syndrome | Giant Axonal Neuropathy | Periventricular Nodular Heterotopia | Familial Hypertrophic Cardiomyopathy | Ophthalmia, Sympathetic | Acne | Autosomal Recessive Spastic Paraplegia Type 75 | Congenital Mirror Movements