recessive
234 results
101 - 200- proteinosis
- deficiency
- Adrenal Crisis, Acute
- gene
- Salla disease
- pseudoxanthoma
- Antley-Bixler syndrome
- Farber disease
- hyperekplexia, hyperexplexia
- neuroacanthosis
- hypoplasia
- mitochondrial disease
- Hemophilia
- Wolman disease
- ochronosis
- hyperplasia
- fetal akinesia deformation sequence
- immotile cilia syndrome
- Papillon-Lefèvre syndrome
- cystinosis
- Cystic Fibrosis
- Pyruvate Kinase
- disease
- Laurence-Moon-Biedl syndrome
- Becker muscular dystrophy
- Bernard-Soulier syndrome
- juvenile hemochromatosis
- carrier screening, carrier identification
- uniparental disomy
- ataxia-telangiectasia
- Chédiak-Higashi syndrome
- Glanzmann thrombasthenia
- hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
- Smith-Lemli-Opitz syndrome
- Bietti crystalline dystrophy
- xeroderma
- dominant
- Osteomyelitis
- Premature Rupture of Membranes
- Duchenne, Guillaume B. A.
- neuronal ceroid lipofuscinosis
- Zellweger syndrome
- Glomerulonephritis, Acute
- Urinary Tract Infection
- Refsum disease
- Platelet Count and Tests of Platelet Function
- Charcot-Marie-Tooth disease
- Crigler-Najjar syndrome
- epidermodysplasia verruciformis
- Esophageal Cancer
- Glaucoma
- Iron Deficiency Anemia
- Hyperlipoproteinemia
- Hypothyroidism
- pyknodysostosis
- hypophosphatasia
- atrophy
- fever
- Polycystic Kidney Disease
- Bilirubin and Bilirubin Fractions
- Batten disease
- Laron, Zvi
- Abdominal Aortic Aneurysm
- Hyperthyroidism
- Liver Failure
- Myasthenia Gravis
- Ventricular Dysrhythmias
- Niemann-Pick disease
- Mendel laws
- blue diaper syndrome
- Amyloidosis
- Atrial Dysrhythmias
- Bone Cancer
- Hypochloremia
- Multiple Sclerosis
- myotonia
- Muscular Dystrophy
- Parkinson Disease
- Plasminogen and Tissue Plasminogen Activator Antigen
- Ceruloplasmin
- carrier
- ichthyosis
- Pulmonary Hypertension
- Sickle Cell Disease
- Copper
- Oguchi disease
- Biopsy, Chorionic Villus
- Glucose-6-Phosphate Dehydrogenase
- galactosemia
- osteopetrosis
- Dent disease
- Porphyrins, Blood and Urine
- chromosome
- chronic granulomatous disease
- hemoglobin C disease