GeneReviews
0-9 | 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
- Galactosemia
- GARS-Associated Axonal Neuropathy
- GATA1-Related Cytopenia
- Gaucher Disease
- Geleophysic Dysplasia
- Genetic Prion Diseases
- Giant Axonal Neuropathy
- Glucose Transporter Type 1 Deficiency Syndrome
- Glycine Encephalopathy
- Glycogen Storage Disease Type I
- Glycogen Storage Disease Type II (Pompe Disease)
- Glycogen Storage Disease Type III
- Glycogen Storage Disease Type IV
- Glycogen Storage Disease Type V
- Glycogen Storage Disease Type VI
- GNE-Related Myopathy
- Greig Cephalopolysyndactyly Syndrome
- GRN-Related Frontotemporal Dementia
- GTP Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia
- Hand-Foot-Genital Syndrome
- Hemophilia A
- Hemophilia B
- Hepatic Veno-occlusive Disease with Immunodeficiency
- Hereditary Ataxias
- Hereditary Coproporphyria
- Hereditary Diffuse Gastric Cancer
- Hereditary Folate Malabsorption
- Hereditary Hearing Loss and Deafness
- Hereditary Hemorrhagic Telangiectasia
- Hereditary Leiomyomatosis and Renal Cell Cancer
- Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum
- Hereditary Multiple Osteochondromas
- Hereditary Neuralgic Amyotrophy
- Hereditary Neuropathy with Liability to Pressure Palsies
- Hereditary Paraganglioma-Pheochromocytoma Syndromes
- Hereditary Sensory and Autonomic Neuropathy Type II
- Hereditary Sensory and Autonomic Neuropathy Type IV
- Hereditary Sensory Neuropathy Type IA
- Hereditary Spastic Paraplegia
- Heritable Pulmonary Arterial Hypertension
- Hermansky-Pudlak Syndrome
- Hexosaminidase A Deficiency
- HFE-Associated Hereditary Hemochromatosis
- Hidrotic Ectodermal Dysplasia 2
- Hirschsprung Disease
- Holoprosencephaly
- Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency
- Huntington Disease
- Huntington Disease-Like 2
- Hutchinson-Gilford Progeria Syndrome
- Hyalinosis, Inherited Systemic
- Hyperekplexia
- Hyperkalemic Periodic Paralysis Type 1
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
- Hyperoxaluria, Primary, Type 1
- Hyperoxaluria, Primary, Type 2
- Hypochondroplasia
- Hypohidrotic Ectodermal Dysplasia
- Hypokalemic Periodic Paralysis
- Hypomyelination and Congenital Cataract
- Hypophosphatasia