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Meet Thalon (10948)
New Donor
Thalon is a thoughtful, creative soul with a deep love for music. Standing at 6 feet tall with warm, sparkling, brown-green eyes and a bright, genuine smile, he has such a joyful, infectious energy that really shines. His hair has a wonderful natural texture; it's thick and wavy with a lovely bounce to it that gives him a youthful, dynamic look. The curls frame his face in a way that's both casual and charming. His style gives off a perfect casual-but-put-together vibe that's both practical and polished.
Raised in a musically gifted family, Thalon grew up surrounded by harmony, literally and figuratively, and has carried that passion into his adult life as a composer, performer, and sound designer. With a degree in Arts, Media & Engineering, he blends technical skill with artistic intuition, crafting music that’s rich and emotionally resonant. He’s a lifelong learner, a patient listener, and someone who finds joy in nature, biking, and meaningful conversation. Whether he's composing a new piece or simply sharing a moment with loved ones, he brings sincerity, resilience, and a deep respect for the human experience.
Brown/Green
Dark Brown
6'00"
165
O Rh+
-
Caucasian, German, Norwegian
No
B.A. on Bachelor's in Arts, Media and Engineering / Market Hand, Composer
No
Fulgent Beacon 515 Panel
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- No disease causing mutations detected
 
 
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- Karyotyping : 46,XY
 
 
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- Karyotyping
 - Cystic Fibrosis
 - Adenosine Deaminase Deficiency
 - ABCC8-related Hyperinsulinism
 - Achromatopsia
 - Alpha-mannosidosis
 - Andermann Syndrome
 - Argininosuccinic Aciduria
 - ARSACS
 - Aspartylglycosaminuria
 - Ataxia With Vitamin E Deficiency
 - Ataxia-telangiectasia
 - Autosomal Recessive Polycystic Kidney Disease
 - Bardet-Biedl Syndrome, BBS1-related
 - Bardet-Biedl Syndrome, BBS10-related
 - Bloom Syndrome
 - Canavan Disease
 - Carnitine Palmitoyltransferase IA Deficiency
 - Carnitine Palmitoyltransferase II Deficiency
 - Cartilage-hair Hypoplasia
 - Citrullinemia Type 1
 - CLN3-related Neuronal Ceroid Lipofuscinosis
 - CLN5-related Neuronal Ceroid Lipofuscinosis
 - CLN8-related Neuronal Ceroid Lipofuscinosis
 - Cohen Syndrome
 - 21-hydroxylase Deficient Congenital Adrenal Hyperplasia
 - Congenital Disorder Of Glycosylation Type Ia
 - Congenital Disorder Of Glycosylation Type Ib
 - Costeff Optic Atrophy Syndrome
 - Cystinosis
 - D-bifunctional Protein Deficiency
 - Dihydrolipoamide Dehydrogenase Deficiency
 - Ethylmalonic Encephalopathy
 - Fanconi Anemia Type C
 - Galactosemia
 - Gaucher Disease
 - GJB2-related DFNB1 Nonsyndromic Hearing Loss And Deafness
 - Glutaric Acidemia Type 1
 - Glutathione Synthetase Deficiency
 - Glycogen Storage Disease Type Ia
 - Glycogen Storage Disease Type Ib
 - Glycogen Storage Disease Type II
 - Glycogen Storage Disease Type III
 - Glycogen Storage Disease Type V
 - GRACILE Syndrome
 - Hb Beta Chain-related Hemoglobinopathy (including Beta Thalassemia And Sickle Cell Disease)
 - Hereditary Fructose Intolerance
 - HMG-CoA Lyase Deficiency
 - Holocarboxylase Synthetase Deficiency
 - Hexosaminidase A Deficiency (including Tay-Sachs Disease)
 - Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
 - Hypophosphatasia, Autosomal Recessive
 - Inclusion Body Myopathy 2
 - Isovaleric Acidemia
 - Joubert Syndrome 2
 - Junctional Epidermolysis Bullosa, LAMA3-related
 - Junctional Epidermolysis Bullosa, LAMB3-related
 - Junctional Epidermolysis Bullosa, LAMC2-related
 - Krabbe Disease
 - Limb-girdle Muscular Dystrophy Type 2D
 - Limb-girdle Muscular Dystrophy Type 2E
 - Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
 - Maple Syrup Urine Disease Type 1A
 - Maple Syrup Urine Disease Type 1B
 - Medium Chain Acyl-CoA Dehydrogenase Deficiency
 - Megalencephalic Leukoencephalopathy With Subcortical Cysts
 - Metachromatic Leukodystrophy
 - Methylmalonic Acidemia MMAA-related
 - Methylmalonic Acidemia MMAB-related
 - Methylmalonic Acidemia MUT-related
 - Methylmalonic Aciduria And Homocystinuria Type CbIC
 - MTHFR Deficiency
 - Mucolipidosis IV
 - Mucopolysaccharidosis Type I
 - Muscle-eye-brain Disease
 - NEB-related Nemaline Myopathy
 - Niemann-Pick Disease, SMPD1-associated
 - Nijmegen Breakage Syndrome
 - Pendred Syndrome
 - PEX1-related Zellweger Syndrome Spectrum
 - Phenylalanine Hydroxylase Deficiency
 - Polyglandular Autoimmune Syndrome Type 1
 - PPT1-related Neuronal Ceroid Lipofuscinosis
 - Primary Carnitine Deficiency
 - Primary Hyperoxaluria Type 1
 - Primary Hyperoxaluria Type 2
 - Propionic Acidemia, PCCA-Related
 - Propionic Acidemia, PCCB-Related
 - PROP1-related Combined Pituitary Hormone Deficiency
 - Pycnodysostosis
 - Rhizomelic Chondrodysplasia Punctata Type 1
 - Salla Disease
 - Sandhoff Disease
 - Segawa Syndrome
 - Sjogren-Larsson Syndrome
 - Smith-Lemli-Opitz Syndrome
 - Sulfate Transporter-related Osteochondrodysplasia (SLC26A2)
 - TPP1-related Neuronal Ceroid Lipofuscinosis
 - Tyrosinemia Type I
 - Usher Syndrome Type 1F
 - Usher Syndrome Type 3
 - Very Long Chain Acyl-CoA Dehydrogenase Deficiency
 - Walker-Warburg Syndrome
 - Wilson Disease
 - Maple Syrup Urine Disease Type II
 - 6-pyruvoyl-tetrahydropterin Synthase Deficiency
 - 11-beta-hydroxylase-deficient Congenital Adrenal Hyperplasia
 - Alstrom Syndrome
 - AMT-related Glycine Encephalopathy
 - Argininemia
 - Autosomal Recessive Osteopetrosis Type 1
 - Bardet-Biedl Syndrome, BBS12-related
 - Bardet-Biedl Syndrome, BBS2-related
 - Calpainopathy
 - Carbamoylphosphate Synthetase I Deficiency
 - Cerebrotendinous Xanthomatosis
 - CLN6-related Neuronal Ceroid Lipofuscinosis
 - COL4A3-related Alport Syndrome
 - COL4A4-related Alport Syndrome
 - Congenital Disorder Of Glycosylation Type Ic
 - Delta-sarcoglycanopathy
 - Dysferlinopathy
 - ERCC6-related Disorders
 - ERCC8-related Disorders
 - EVC-related Ellis-van Creveld Syndrome
 - EVC2-related Ellis-van Creveld Syndrome
 - Fanconi Anemia Complementation Group A
 - FKRP-related Disorders
 - Galactokinase Deficiency
 - Gamma-sarcoglycanopathy
 - GLB1-related Disorders
 - GLDC-related Glycine Encephalopathy
 - GNPTAB-related Disorders
 - Hydrolethalus Syndrome
 - KCNJ11-related Familial Hyperinsulinism
 - LAMA2-related Muscular Dystrophy
 - Leigh Syndrome, French-Canadian Type
 - Lipoid Congenital Adrenal Hyperplasia
 - Lysosomal Acid Lipase Deficiency
 - MKS1-related Disorders
 - Mucolipidosis III Gamma
 - Mucopolysaccharidosis Type IIIA
 - Mucopolysaccharidosis Type IIIB
 - Mucopolysaccharidosis Type IIIC
 - MYO7A-related Disorders
 - Niemann-Pick Disease Type C2
 - Peroxisome Biogenesis Disorder Type 3
 - Peroxisome Biogenesis Disorder Type 4
 - Peroxisome Biogenesis Disorder Type 5
 - Peroxisome Biogenesis Disorder Type 6
 - Primary Hyperoxaluria Type 3
 - Pyruvate Carboxylase Deficiency
 - RTEL1-related Disorders
 - Spastic Paraplegia Type 15
 - Spondylothoracic Dysostosis
 - TGM1-related Autosomal Recessive Congenital Ichthyosis
 - Tyrosinemia Type II
 - USH1C-related Disorders
 - USH2A-related Disorders
 - Xeroderma Pigmentosum Group A
 - Xeroderma Pigmentosum Group C
 - 3-Beta-Hydroxysteroid Dehydrogenase Type II Deficiency
 - 3-Phosphoglycerate Dehydrogenase Deficiency (PHGDH)
 - Abetalipoproteinemia (MTTP)
 - Achalasia-addisonianism-alacrimia Syndrome
 - Acrodermatitis Enteropathica
 - Acute Infantile Liver Failure
 - Acyl-CoA Oxidase I Deficiency
 - Aicardi-Gouti?res Syndrome (SAMHD1-Related)
 - Aicardi-Goutieres Syndrome (RNASEH2C-related)
 - Aicardi-Goutieres Syndrome 1 (and Other TREX1-related Retinal Dystroph
 - Angelman Syndrome
 - Anterior Segment Dysgenesis (CYP1B1-related) / Glaucoma (CYP1B1-relate
 - Antley-Bixler Syndrome (POR-related)
 - Aromatase Deficiency
 - Arthrogryposis, Mental Retardation, And Seizures (SLC35A3)
 - Asparagine Synthetase Deficiency
 - Ataxia-Telangiectasia-Like Disorder (MRE11)
 - Bardet-Biedl Syndrome (ARL6-related)
 - Bardet-Biedl Syndrome (BBS4-related)
 - Bardet-Biedl Syndrome (TRIM32-related)
 - Bare Lymphocyte Syndrome, Type II
 - Bartter Syndrome, Type 4A
 - Beta-Ketothiolase Deficiency
 - Beta-mannosidosis
 - BH4-deficient Hyperphenylalaninemia C
 - BH4-deficient Hyperphenylalaninemia D
 - Carnitine Acylcarnitine Translocase Deficiency
 - Carpenter Syndrome
 - Catecholaminergic Polymorphic Ventricular Tachycardia
 - CD59-mediated Hemolytic Anemia
 - Cerebral Creatine Deficiency Syndrome 2
 - Cerebral Creatine Deficiency Syndrome 3
 - Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratode
 - Charcot-Marie-Tooth Disease, Type 4D
 - Chediak-Higashi Syndrome
 - Choreoacanthocytosis
 - Chronic Granulomatous Disease (CYBA-related)
 - Citrin Deficiency
 - Combined Malonic And Methylmalonic Aciduria
 - Combined Oxidative Phosphorylation Deficiency 1
 - Combined Oxidative Phosphorylation Deficiency 3
 - Combined Pituitary Hormone Deficiency 1
 - Combined Pituitary Hormone Deficiency 3
 - Combined SAP Deficiency
 - Congenital Adrenal Hyperplasia Due To 17-Alpha-Hydroxylase Deficiency
 - Congenital Adrenal Insufficiency (CYP11A1-related)
 - Congenital Amegakaryocytic Thrombocytopenia (MPL)
 - Congenital Disorder Of Deglycosylation
 - Congenital Dyserythropoietic Anemia Type 2
 - Congenital Ichthyosis 4A And 4B
 - Congenital Insensitivity To Pain With Anhidrosis
 - Congenital Myasthenic Syndrome (CHAT-related)
 - Congenital Myasthenic Syndrome (CHRNE-Related)
 - Congenital Myasthenic Syndrome (DOK7-related)
 - Congenital Myasthenic Syndrome (RAPSN-Related)
 - Congenital Neutropenia (HAX1-Related)
 - Congenital Neutropenia (VPS45-Related)
 - Congenital Nongoitrous Hypothryoidism 1 / Nonautoimmune Hyperthyroidis
 - Congenital Nongoitrous Hypothryoidism 4
 - Congenital Secretory Chloride Diarrhea 1
 - Corneal Dystrophy And Perceptive Deafness
 - Corticosterone Methyloxidase Deficiency
 - Cytochrome C Oxidase Deficiency / Leigh Syndrome (COX15-related)
 - Deafness, Autosomal Recessive 3
 - Deafness, Autosomal Recessive 59
 - Deafness, Autosomal Recessive 7 / Deafness, Autosomal Dominant 36
 - Deafness, Autosomal Recessive 76
 - Deafness, Autosomal Recessive 77
 - Deafness, Autosomal Recessive 8
 - Deafness, Autosomal Recessive 9 / Auditory Neuropathy
 - Desbuquois Dysplasia 1
 - Dystrophic Epidermolysis Bullosa
 - Ehlers-Danlos Syndrome, Type VI
 - Ehlers-Danlos Syndrome, Type VIIC
 - Enhanced S-Cone Syndrome
 - Familial Autosomal Recessive Hypercholesterolemia
 - Familial Hypercholesterolemia (LDLR-related)
 - Familial Hyperinsulinemic Hypoglycemia 4 / 3-Hydroxyacyl-CoA Dehydroge
 - Familial Hyperphosphatemic Tumoral Calcinosis
 - Fanconi Anemia, Group G
 - Fructose-1,6-Bisphosphatase Deficiency
 - Fucosidosis
 - Galactose Epimerase Deficiency
 - Galactosialidosis
 - Geroderma Osteodysplasticum
 - Gitelman Syndrome
 - Glanzmann Thrombasthenia (ITGB3-related)
 - Glutaric Acidemia, Type IIa
 - Glutaric Acidemia, Type IIb
 - Glutaric Acidemia, Type IIc
 - Glycogen Storage Disease, Type IV / Adult Polyglucosan Body Disease
 - Glycogen Storage Disease, Type IXb
 - Glycogen Storage Disease, Type VII
 - Hawkinsinuria / Tyrosinemia, Type III
 - Hemochromatosis, Type 3
 - Hereditary Leiomyomatosis And Renal Cell Cancer / Fumarase Deficiency
 - Hereditary Spastic Paraparesis 49
 - Hermansky-Pudlak Syndrome (HPS4-related)
 - Hermansky-Pudlak Syndrome (HPS6-related)
 - Hermansky-Pudlak Syndrome, Type 1
 - Hermansky-Pudlak Syndrome, Type 3
 - Homocystinuria, CblE Type
 - Homocystinuria-Megaloblastic Anemia, Cobalamin G Type
 - Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
 - Hypoparathyroidism-retardation-dysmorphic Syndrome
 - Immunodeficiency 18
 - Immunodeficiency 19
 - Infantile Cerebral And Cerebellar Atrophy
 - Infantile Neuroaxonal Dystrophy 1 And Other PLA2G6-related Disorders
 - Intrahepatic Cholestasis
 - Joubert Syndrome (and Other NPHP1-related Ciliopathies)
 - Joubert Syndrome 7 / Meckel Syndrome 5 / COACH Syndrome
 - Junctional Epidermolysis Bullosa (COL17A1-related)
 - Junctional Epidermolysis Bullosa (ITGA6-related)
 - Junctional Epidermolysis Bullosa (ITGB4-related)
 - Laron Dwarfism
 - Leber Congenital Amaurosis (and Other AIPL1-related Ciliopathies)
 - Leber Congenital Amaurosis (and Other GUCY2D-related Ciliopathies)
 - Leber Congenital Amaurosis (and Other TULP1-related Retinopathies)
 - Leber Congenital Amaurosis 10 And Other CEP290-Related Ciliopathies
 - Leber Congenital Amaurosis 13
 - Leber Congenital Amaurosis 2 / Retinitis Pigmentosa 20
 - Leber Congenital Amaurosis 5
 - Leber Congenital Amaurosis 8 / Retinitis Pigmentosa 12 / Pigmented Par
 - Leigh Syndrome (NDUFS7-related)
 - Leigh Syndrome (SURF1-related)
 - Lethal Congenital Contracture Syndrome 1 / Lethal Arthrogryposis With
 - Leukoencephalopathy With Vanishing White Matter
 - Lipoprotein Lipase Deficiency
 - Lysinuric Protein Intolerance
 - Malonyl-CoA Decarboxylase Deficiency
 - MEDNIK Syndrome
 - Megaloblastic Anemia 1
 - Mental Retardation, Autosomal Recessive 3
 - Methylmalonic Aciduria And Homocystinuria, Cobalamin D Type
 - Methylmalonic Aciduria And Homocystinuria, Cobalamin F Type
 - Methylmalonyl-CoA Epimerase Deficiency
 - Microcephaly 9, Primary, AR / Seckel Syndrome 5 (CEP152-related)
 - Microphthalmia / Anophthalmia
 - Mitochondrial Complex I Deficiency (ACAD9-Related)
 - Mitochondrial Complex I Deficiency (NDUFAF5-Related)
 - Mitochondrial Complex I Deficiency (NDUFS6-Related)
 - Mitochondrial Complex I Deficiency (NDUFV1-related)
 - Mitochondrial Complex I Deficiency / Leigh Syndrome (FOXRED1-related)
 - Mitochondrial Complex I Deficiency / Leigh Syndrome (NDUFAF2-related)
 - Mitochondrial Complex I Deficiency / Leigh Syndrome (NDUFS4-related)
 - Mitochondrial Complex IV Deficiency (PET100-related)
 - Mitochondrial DNA Depletion Syndrome 2
 - Mitochondrial DNA Depletion Syndrome 3
 - Mitochondrial DNA Depletion Syndrome 4A And 4B And Other POLG-related
 - Mitochondrial DNA Depletion Syndrome 6 / Navajo Neurohepatopathy
 - Mitochondrial Myopathy And Sideroblastic Anemia 1
 - Mitochondrial Trifunctional Protein Deficiency (HADHB-Related)
 - Molybdenum Cofactor Deficiency A
 - Mucopolysaccharidosis Type IIID
 - Mucopolysaccharidosis Type IVa
 - Mucopolysaccharidosis Type VI
 - Mucopolysaccharidosis VII
 - Mucopolysaccharidosis?type IX
 - Mulibrey Nanism
 - Multiple Congenital Anomalies-hypotonia-seizures Syndrome 1
 - Multiple Pterygium Syndrome
 - Multiple Sulfatase Deficiency (SUMF1)
 - Myoneurogastrointestinal Encephalopathy
 - N-Acetylglutamate Synthase Deficiency
 - Nephrogenic Diabetes Insipidus, Type II
 - Nephronophthisis 2
 - Neuronal Ceroid-Lipofuscinosis (MFSD8-Related)
 - Niemann-Pick Disease, Type C (NPC1-Related)
 - Oculocutaneous Albinism (SLC45A2-related)
 - Oculocutaneous Albinism (TYR-related)
 - Oculocutaneous Albinism (TYRP1-related)
 - Odonto-Onycho-Dermal Dysplasia / Schopf-Schulz-Passarge Syndrome
 - Omenn Syndrome (RAG2-Related)
 - Omenn Syndrome / Severe Combined Immunodeficiency, Athabaskan-Type
 - Omenn Syndrome And Other RAG1-related Disorders
 - Ornithine Aminotransferase Deficiency
 - Osteogenesis Imperfecta, Type XI
 - Papillon-Lefevre Syndrome
 - Peroxisome Biogenesis Disorder 7A And 7B
 - Pontocerebellar Hypoplasia, Type 1A
 - Pontocerebellar Hypoplasia, Type 1B
 - Pontocerebellar Hypoplasia, Type 2A And Type 4
 - Pontocerebellar Hypoplasia, Type 2E
 - Pontocerebellar Hypoplasia, Type 6
 - Primary Ciliary Dyskinesia (CCDC103-related)
 - Primary Ciliary Dyskinesia (CCDC39-related)
 - Primary Ciliary Dyskinesia (DNAH5-Related)
 - Primary Ciliary Dyskinesia (DNAI1-Related)
 - Primary Ciliary Dyskinesia (DNAI2-related)
 - Progressive Cerebello-Cerebral Atrophy
 - Progressive Familial Intrahepatic Cholestasis, Type 2
 - Progressive Pseudorheumatoid Dysplasia
 - Prolidase Deficiency
 - Pulmonary Surfactant Dysfunction
 - Pyridoxamine 5'-Phosphate Oxidase Deficiency
 - Pyridoxine-Dependent Epilepsy
 - Pyruvate Dehydrogenase E1-Beta Deficiency
 - Renal Tubular Acidosis And Deafness
 - Retinitis Pigmentosa 25
 - Retinitis Pigmentosa 26
 - Retinitis Pigmentosa 28
 - Retinitis Pigmentosa 36
 - Retinitis Pigmentosa 59 (DHDDS)
 - Rhizomelic Chondrodysplasia Punctata, Type 3
 - Roberts Syndrome
 - Salt And Pepper Developmental Regression Syndrome
 - Schimke Immunoosseous Dysplasia
 - Sepiapterin Reductase Deficiency
 - Severe Combined Immunodeficiency (IL7R-Related)
 - Severe Combined Immunodeficiency (JAK3-related)
 - Severe Combined Immunodeficiency (PTPRC-related)
 - Severe Congenital Neutropenia 4
 - Sialidosis, Type I And Type II
 - Spastic Tetraplegia, Thin Corpus Callosum, And Progressive Microcephal
 - Spinal Muscular Atrophy With Respiratory Distress 1 / Charcot-Marie-To
 - Spondylocostal Dysostosis 1
 - Steel Syndrome
 - Stickler Syndrome (and Other COL11A2 Related Deafness Disorders)
 - Stuve-Wiedemann Syndrome
 - Thiamine-responsive Megaloblastic Anemia Syndrome
 - Thyroid Dyshormonogenesis 1
 - Thyroid Dyshormonogenesis 2A
 - Thyroid Dyshormonogenesis 3
 - Thyroid Dyshormonogenesis 6
 - Trichohepatoenteric Syndrome 1
 - Usher Syndrome, Type ID
 - Vitamin D-dependent Rickets, Type I
 - Vitamin D-resistant Rickets, Type IIA
 - Werner Syndrome
 - Wolcott-Rallison Syndrome
 - Woodhouse-Sakati Syndrome
 - Xeroderma Pigmentosum Variant (POLH-related)
 - Nephrotic Syndrome (NPHS1-Related)
 - Nephrotic Syndrome (NPHS2-Related)
 - RYR1-related Diseases
 - TMEM67-related Conditions
 - ABCA4-related Conditions
 - Trimethylaminuria
 - Leukoencephalopathy With Vanishing White Matter
 - Progressive Familial Intrahepatic Cholestasis 3 (ABCB4)
 - Dubin-Johnson Syndrome (ABCC2)
 - Isolated Ectopia Lentis (ADAMTSL4)
 - Polymicrogyria (ADGRG1)
 - ADGRV1-related Conditions (ADGRV1)
 - AHI1-related Conditions (AHI1)
 - Congenital Disorder Of Glycosylation Type Ik (ALG1)
 - Spinocerebellar Ataxia (ANO10)
 - BBS5-related Conditions (BBS5)
 - Bardet-Biedl Syndrome (BBS7)
 - Bardet-Biedl Syndrome (BBS9)
 - Hermansky-Pudlak Syndrome Type 8 (BLOC1S3)
 - Hermansky-Pudlak Syndrome Type 9 (BLOC1S6)
 - Osteogenesis Imperfecta (BMP1)
 - BRIP1-related Conditions (BRIP1)
 - Developmental And Epileptic Encephalopathy (CAD)
 - CC2D2A-related Conditions (CC2D2A)
 - Congenital Hydrocephalus-1 (CCDC88C)
 - Hyper-IgM Immunodeficiency (CD40)
 - Myotonia Congenita (CLCN1)
 - Osteogenesis Imperfecta (CRTAP)
 - Neuronal Ceroid Lipofuscinosis Type 10 (CTSD)
 - CYP7B1-related Conditions (CYP7B1)
 - Warsaw Syndrome
 - Congenital Chronic Diarrhea (DGAT1)
 - Primary Ciliary Dyskinesia (DNAH11)
 - Immunodeficiency-centromeric Instability-facial Anomalies Syndrome 1 (DNMT3B)
 - DYNC2H1-related Conditions (DYNC2H1)
 - Leukoencephalopathy With Vanishing White Matter (EIF2B1)
 - Leukoencephalopathy With Vanishing White Matter (EIF2B3)
 - Leukoencephalopathy With Vanishing White Matter (EIF2B4)
 - Familial Dysautonomia (ELP1)
 - Vici Syndrome
 - Xeroderma Pigmentosum, Group G
 - Fanconi Anemia Type D2 (FANCD2)
 - Fanconi Anemia Type E (FANCE)
 - Fanconi Anemia Type I (FANCI)
 - Fanconi Anemia Type L (FANCL)
 - Parkinson Disease 15 (FBXO7)
 - Severe Combined Immunodeficiency Due To FOXN1 deficiency (FOXN1)
 - Fraser Syndrome (FRAS1)
 - Fraser Syndrome (FREM2)
 - GCH1-related Conditions (GCH1)
 - GDF5-related Conditions (GDF5)
 - Retinitis Pigmentosa 36 (GNPAT)
 - Fraser Syndrome (GRIP1)
 - Hereditary Hemochromatosis Type 2 (HAMP)
 - Hereditary Hemochromatosis Type 2 (HJV)
 - Geme Oxygenase 1 Deficiency (HMOX1)
 - Hermansky-Pudlak Syndrome Type 5 (HPS5)
 - 17-beta Hydroxysteroid Dehydrogenase 3 Deficiency (HSD17B3)
 - Combined Immunodeficiency Due To IKBKB deficiency (IKBKB)
 - Bartter Syndrome Type 2 (KCNJ1)
 - Muscular Dystrophy-dystroglycanopathy (LARGE1)
 - LIG4 syndrome (LIG4)
 - LRAT-related Conditions (LRAT)
 - Donnai-Barrow Syndrome (LRP2)
 - Retinitis Pigmentosa 62 (MAK)
 - Primary Microcephaly
 - Childhood-onset Dystonia With Optic Atrophy And Basal Ganglia Abnormalities (MECR)
 - MKKS-related Conditions (MKKS)
 - Molybdenum Cofactor Deficiency (MOCS2)
 - MUSK-related Conditions (MUSK)
 - MVK-related Conditions (MVK)
 - Alpha-N-acetylgalactosaminidase Deficiency (NAGA)
 - Chronic Granulomatous Disease (NCF2)
 - NSMCE3 deficiency (NSMCE3)
 - Oculocutaneous Albinism Type 2 OCA2)
 - OSTM1 deficiency Associated Osteopetrosis (OSTM1)
 - OTOF-related Conditions (OTOF)
 - Osteogenesis Imperfecta (P3H1)
 - Pantothenate Kinase-associated Neurodegeneration (PANK2)
 - Microcephalic Osteodysplastic Primordial Dwarfism Type II (PCNT)
 - Zellweger Spectrum Disorder (PEX13-related)
 - Zellweger Spectrum Disorder (PEX16-related)
 - PEX5-related Conditions (PEX5)
 - PGM3-congenital Disorder Of Glycosylation (PGM3)
 - Glycogen Storage Disease Type IXc (PHKG2)
 - Refsum Disease (PHYH)
 - PLEKHG5-related Conditions (PLEKHG5)
 - Muscular Dystrophy-dystroglycanopathy (POMT1)
 - Muscular Dystrophy-dystroglycanopathy (POMT2)
 - Brittle Cornea Syndrome (PRDM5-related)
 - Familial Hemophagocytic Lymphohistiocytosis Type 2 (PRF1)
 - RLBP1-related Conditions (RLBP1)
 - Aicardi-Goutieres Syndrome 4
 - Aicardi-Goutieres Syndrome 2
 - Muscular Dystrophy-dystroglycanopathy (RXYLT1)
 - SAMD9-related Conditions (SAMD9)
 - Cardioencephalomyopathy (SCO2)
 - Trichohepatoenteric Syndrome (SKIV2L)
 - Bartter Syndrome Type 1 (SLC12A1)
 - Biotin-responsive Basal Ganglia Disease (SLC19A3)
 - Ichthyosis Prematurity Syndrome (SLC27A4)
 - Foveal Hypoplasia (SLC38A8)
 - SPG11-related Conditions (SPG11)
 - Steroid 5-alpha-reductase Deficiency (SRD5A2)
 - Familial Hemophagocytic Lymphohistiocytosis Type 4 (STX11)
 - Familial Hemophagocytic Lymphohistiocytosis Type 5 (STXBP2)
 - Sulfite Oxidase Deficiency (SUOX)
 - Metabolic Crises With Rhabdomyolysis, Cardiac Arrhythmias And Neurodegeneration (TANGO2)
 - Progressive Early-onset Encepahlopathy With Brain Atrophy And Thin Corpus Callosum (PEBAT) (TBCD)
 - Transcobalamin II Deficiency (TCN2)
 - Dyskeratosis Congenita Spectrum Disorders (TERT)
 - Atransferrinemia (TF)
 - Johanson-Blizzard Syndrome (UBR1)
 - Familial Hemophagocytic Lymphohistiocytosis Type 3 (UNC13D)
 - Cerebellar Ataxia, Intellectual Disability, And Dysequilibrium Syndrome 1 (VLDLR)
 - Immunodeficiency-centromeric Instability-facial Anomalies Syndrome 2 (ZBTB24)
 - Brittle Cornea Syndrome (ZNF469)
 - GJB6-CRYL1 Related Nonsyndromic Hearing Loss UK
 - GJB6-CRYL1 Related Nonsyndromic Hearing Loss