general/autosomal-dominant-disorders

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Polydactyly

Physical anomaly involving extra fingers or toes

general/autosomal-dominant-disorders
Aromatase excess syndrome
general/autosomal-dominant-disorders
3-Methylcrotonyl-CoA carboxylase deficiency
general/autosomal-dominant-disorders
Autosomal dominant cerebellar ataxia
general/autosomal-dominant-disorders
Bethlem myopathy
general/autosomal-dominant-disorders
Buschke–Ollendorff syndrome

Genetic disorder involving small, painless lumps on the skin

general/autosomal-dominant-disorders
Familial atrial fibrillation
general/autosomal-dominant-disorders
Gray platelet syndrome
general/autosomal-dominant-disorders
Hereditary elliptocytosis

Genetic haematological condition

general/autosomal-dominant-disorders
MOMO syndrome

Rare genetic disorder

general/autosomal-dominant-disorders
Medullary cystic kidney disease
general/autosomal-dominant-disorders
Hereditary mucoepithelial dysplasia
general/autosomal-dominant-disorders
Miller–Dieker syndrome

Genetic disorder

general/autosomal-dominant-disorders
Keratolytic winter erythema

Genetic disorder causing redness and peeling of the skin on the palms and soles

general/autosomal-dominant-disorders
Langer–Giedion syndrome
general/autosomal-dominant-disorders
PAPA syndrome

Genetic disorder in humans

general/autosomal-dominant-disorders
Parastremmatic dwarfism
general/autosomal-dominant-disorders
Gillespie syndrome
general/autosomal-dominant-disorders
Platyspondylic lethal skeletal dysplasia, Torrance type
general/autosomal-dominant-disorders
Stickler syndrome

Genetic connective tissue disorder

general/autosomal-dominant-disorders
Von Hippel–Lindau disease
general/autosomal-dominant-disorders
Spondyloepiphyseal dysplasia congenita
general/autosomal-dominant-disorders
Pelger–Huët anomaly
general/autosomal-dominant-disorders
Spinal muscular atrophy with lower extremity predominance 1

Rare neuromuscular disorder of infants characterised by severe progressive muscle atrophy

general/autosomal-dominant-disorders
Worth syndrome
general/autosomal-dominant-disorders
Singleton Merten syndrome
general/autosomal-dominant-disorders
Zimmermann–Laband syndrome
general/autosomal-dominant-disorders
Weaver syndrome

Rare genetic overgrowth disorder

general/autosomal-dominant-disorders
Collagenopathy, types II and XI

Group of connective tissue conditions

general/autosomal-dominant-disorders
Felty's syndrome

Autoimmune disease

general/autosomal-dominant-disorders
Roussy–Lévy syndrome
general/autosomal-dominant-disorders
Tricho-rhino-phalangeal syndrome Type 1
general/autosomal-dominant-disorders
Albright's hereditary osteodystrophy

Form of osteodystrophy and a rare human disease

general/autosomal-dominant-disorders
Adermatoglyphia

Rare genetic disorder causing lack of fingerprints

general/autosomal-dominant-disorders
Liddle's syndrome
general/autosomal-dominant-disorders
Von Willebrand disease
general/autosomal-dominant-disorders
Vitelliform macular dystrophy
general/autosomal-dominant-disorders