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SRDCE, DKK, DLK, PATELLY, OCD RAMEN, ODC LOKTŮ, SPONDYLÓZA, ATAXIE, ICHTYÓZA, PROGRESSIVE RETINAL ATROPHY, CRD1, CANINE MULTIFOCAL RETINOPATHY, CMR1, HYPERURICOSURIA AND HYPERURICEMIA OR UROLITHIASIS, HUU, NEURONAL CEROID LIPOFUSCINOSIS, CEREBELLAR ATAXIA, NCL4A, NEURONAL CEROID LIPOFUSCINOSIS 10, NCL 10, L-2-HYDROXYGLUTARICACIDURIA, L2HGA, PRIMARY LENS LUXATION, PECTINATE LIGAMENT DYSPLASIA, PLD, EYE ANOMALY, CHOROIDAL HYPOPLASIA, CEA, DAY BLINDNESS, CONE DEGENERATION, ACHROMATOPSIA, ACHROMATOPSIA, AUTOSOMAL DOMINANT PROGRESSIVE RETINAL ATROPHY, CMR2, CANINE MULTIFOCAL RETINOPATHY, CMR3, PRIMARY OPEN ANGLE GLAUCOMA, MDR1 DRUG SENSITIVITY, P2Y12 RECEPTOR PLATELET DISORDER, FACTOR IX DEFICIENCY, HEMOPHILIA B, FACTOR VII DEFICIENCY, FACTOR VIII DEFICIENCY, HEMOPHILIA A, THROMBOPATHIA, VON WILLEBRAND DISEASE TYPE III, TYPE III VWD, VON WILLEBRAND DISEASE TYPE I, TYPE I VWD, VON WILLEBRAND DISEASE TYPE II, TYPE II VWD, CANINE LEUKOCYTE ADHESION DEFICIENCY TYPE I, CLAD I, CANINE LEUKOCYTE ADHESION DEFICIENCY TYPE III, CLAD III, CONGENITAL MACROTHROMBOCYTOPENIA, CANINE ELLIPTOCYTOSIS, GLANZMANN'S THROMBASTHENIA TYPE I, MAY-HEGGLIN ANOMALY, PREKALLIKREIN DEFICIENCY, PYRUVATE KINASE DEFICIENCYTRAPPED NEUTROPHIL SYNDROME, LIGNEOUS MEMBRANITIS, LMPLATELET FACTOR X RECEPTOR DEFICIENCY, SCOTT SYNDROME, METHEMOGLOBINEMIA, CONGENITAL HYPOTHYROIDISM, COMPLEMENT 3 DEFICIENCY, C3 DEFICIENCY, SEVERE COMBINED IMMUNODEFICIENCY, SCID, X-LINKED SEVERE COMBINED IMMUNODEFICIENCY, X-SCID, PROGRESSIVE RETINAL ATROPHY, RCD1, PROGRESSIVE RETINAL ATROPHY, RCD3, PROGRESSIVE RETINAL ATROPHY, CNGA, PRCD, PRA1, SAG, GR-PRA1, GR-PRA2, CRD4, CORD1, X-LINKED PROGRESSIVE RETINAL ATROPHY 1, XL-PRA1, PRA3, GONIODYSGENESIS, GLAUCOMA, HEREDITARY CATARACTS, EARLY-ONSET CATARACTS, JUVENILE CATARACTS, CONGENITAL STATIONARY NIGHT BLINDNESS, MACULAR CORNEAL DYSTROPHY, MCD, 2,8-DIHYDROXYADENINE UROLITHIASIS, 2,8-DHA UROLITHIASIS, CYSTINURIA TYPE I-A, CYSTINURIA TYPE II-A, CYSTINURIA TYPE II-B, POLYCYSTIC KIDNEY DISEASE, PKD, PRIMARY HYPEROXALURIA, PROTEIN LOSING NEPHROPATHY, PLN, X-LINKED HEREDITARY NEPHROPATHY, XLHN, AUTOSOMAL RECESSIVE HEREDITARY NEPHROPATHY, FAMILIAL NEPHROPATHY, ARHN, PRIMARY CILIARY DYSKINESIA, PCD, CONGENITAL KERATOCONJUNCTIVITIS SICCA AND ICHTHYOSIFORM DERMATOSIS, DRY EYE CURLY COAT SYNDROME, CKCSID, X-LINKED ECTODERMAL DYSPLASIA, ANHIDROTIC ECTODERMAL DYSPLASIA, XHED, RENAL CYSTADENOCARCINOMA AND NODULAR DERMATOFIBROSIS, RCND, CANINE FUCOSIDOSIS, GLYCOGEN STORAGE DISEASE TYPE II, POMPE'S DISEASE, GSD II, GLYCOGEN STORAGE DISEASE TYPE IA, VON GIERKE DISEASE, GSD IA, GLYCOGEN STORAGE DISEASE TYPE IIIA, GSD IIIA, MUCOPOLYSACCHARIDOSIS TYPE IIIA, SANFILIPPO SYNDROME TYPE A, MPS IIIA, MUCOPOLYSACCHARIDOSIS TYPE VII, SLY SYNDROME, MPS VII, GLYCOGEN STORAGE DISEASE TYPE VII, PHOSPHOFRUCTOKINASE DEFICIENCY, PFK DEFICIENCY, LAGOTTO STORAGE DISEASE, NEURONAL CEROID LIPOFUSCINOSIS, NCL 1, 2, 5, 6, 8, 7, ADULT-ONSET NEURONAL CEROID LIPOFUSCINOSIS, NCL A, NCL 12, LATE-ONSET NEURONAL CEROID LIPOFUSCINOSIS, NCL 12, GM1 GANGLIOSIDOSIS, GM2 GANGLIOSIDOSIS, GLOBOID CELL LEUKODYSTROPHY, KRABBE DISEASE, AUTOSOMAL RECESSIVE AMELOGENESIS IMPERFECTA, FAMILIAL ENAMEL HYPOPLASIA, PERSISTENT MULLERIAN DUCT SYNDROME, PMDS, DEAFNESS AND VESTIBULAR SYNDROME, AUTOINFLAMMATORY DISEASE, SPAID, NEONATAL INTERSTITIAL LUNG DISEASE, ENCEPHALOPATHY, SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY, ALEXANDER DISEASE, CEREBELLAR ABIOTROPHY, NEONATAL CEREBELLAR CORTICAL DEGENERATION, NCCD, CEREBELLAR ATAXIA, PROGRESSIVE EARLY-ONSET CEREBELLAR ATAXIA, CEREBELLAR HYPOPLASIA, SPINOCEREBELLAR ATAXIA, LATE-ONSET ATAXIA, LOSCA, SPINOCEREBELLAR ATAXIA WITH MYOKYMIA AND/OR SEIZURES, HEREDITARY ATAXIA, CEREBELLAR DEGENERATION, BENIGN FAMILIAL JUVENILE EPILEPSY, REMITTING FOCAL EPILEPSY, DEGENERATIVE MYELOPATHY, DM, FETAL-ONSET NEONATAL NEUROAXONAL DYSTROPHY, HYPOMYELINATION AND TREMORS, SHAKING PUPPY SYNDROME, X-LINKED GENERALIZED TREMOR SYNDROME, NEUROAXONAL DYSTROPHY, NAD, NEONATAL ENCEPHALOPATHY WITH SEIZURES, NEWS, POLYNEUROPATHY, AMPN, NARCOLEPSY, PROGRESSIVE NEURONAL ABIOTROPHY, CANINE MULTIPLE SYSTEM DEGENERATION, CMSD, JUVENILE LARYNGEAL PARALYSIS AND POLYNEUROPATHY, POLYNEUROPATHY WITH OCULAR ABNORMALITIES AND NEURONAL VACUOLATION, POANV, HEREDITARY SENSORY AUTONOMIC NEUROPATHY, ACRAL MUTILATION SYNDROME, AMS, SENSORY NEUROPATHY, JUVENILE-ONSET POLYNEUROPATHY, LEONBERGER POLYNEUROPATHY 1, LPN1, JUVENILE MYOCLONIC EPILEPSY, JUVENILE-ONSET POLYNEUROPATHY, LEONBERGER POLYNEUROPATHY 2, LPN2, SPONGY DEGENERATION WITH CEREBELLAR ATAXIA 1, SDCA1, SESAME/EAST SYNDROME, SDCA2, DILATED CARDIOMYOPATHY, DCM1, DCM2, LONG QT SYNDROME, CARDIOMYOPATHY AND JUVENILE MORTALITY, MUSCULAR DYSTROPHY, LIMB GIRDLE MUSCULAR DYSTROPHY, ULRICH-LIKE CONGENITAL MUSCULAR DYSTROPHY, CENTRONUCLEAR MYOPATHY, EXERCISE-INDUCED COLLAPSE, INHERITED MYOPATHY, MYOSTATIN DEFICIENCY, BULLY WHIPPET SYNDROME, MYOTONIA CONGENITA, MYOTUBULAR MYOPATHY 1, X-LINKED MYOTUBULAR MYOPATHY, XL-MTM, INFLAMMATORY MYOPATHY, HYPOCATALASIA, ACATALASEMIA, PYRUVATE DEHYDROGENASE DEFICIENCY, MALIGNANT HYPERTHERMIA, IMERSLUND-GRASBECK SYNDROME, SELECTIVE COBALAMIN MALABSORPTION, INHERITED SELECTED COBALAMIN MALABSORPTION WITH PROTEINURIA, LUNDEHUND SYNDROME, CONGENITAL MYASTHENIC SYNDROME, CMS, MYASTHENIA GRAVIS LIKE SYNDROME, EPISODIC FALLING SYNDROME, PAROXYSMAL DYSKINESIA, PXD, DEMYELINATING POLYNEUROPATHY, DYSTROPHIC EPIDERMOLYSIS BULLOSA, ECTODERMAL DYSPLASIA, SKIN FRAGILITY SYNDROME, ICHTHYOSIS, EPIDERMOLYTIC HYPERKERATOSIS, ICHTHYOSIS, ICH1, HEREDITARY FOOTPAD HYPERKERATOSIS, HEREDITARY NASAL PARAKERATOSIS, HNPK, MUSLADIN-LUEKE SYNDROME, MLS, OCULOCUTANEOUS ALBINISM, OCA, BALD THIGH SYNDROME, LETHAL ACRODERMATITIS, LAD, EHLERS DANLOS, CLEFT LIP AND/OR CLEFT PALATE, HEREDITARY VITAMIN D-RESISTANT RICKETS, OCULOSKELETAL DYSPLASIA 2, DWARFISM-RETINAL DYSPLASIA 2, DRD2, OSD2, OSTEOGENESIS IMPERFECTA, BRITTLE BONE DISEASE, OSTEOCHONDRODYSPLASIA, SKELETAL DWARFISM, SKELETAL DYSPLASIA 2, SD2, CRANIOMANDIBULAR OSTEOPATHY, CMO, RAINE SYNDROME, CANINE DENTAL HYPOMINERALIZATION SYNDROME, CHONDRODYSTROPHY AND INTERVERTEBRAL DISC DISEASE, CDDY/IVDD, TYPE I IVDD, CHONDRODYSTROPHY

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