general/autosomal-dominant-disorders
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Polydactyly
Physical anomaly involving extra fingers or toes
Weaver syndrome
Rare genetic overgrowth disorder
Miller–Dieker syndrome
Genetic disorder
PAPA syndrome
Genetic disorder in humans
Keratolytic winter erythema
Genetic disorder causing redness and peeling of the skin on the palms and soles
Stickler syndrome
Genetic connective tissue disorder
Felty's syndrome
Autoimmune disease
Adermatoglyphia
Rare genetic disorder causing lack of fingerprints
Buschke–Ollendorff syndrome
Genetic disorder involving small, painless lumps on the skin
Albright's hereditary osteodystrophy
Form of osteodystrophy and a rare human disease
Spinal muscular atrophy with lower extremity predominance 1
Rare neuromuscular disorder of infants characterised by severe progressive muscle atrophy
MOMO syndrome
Rare genetic disorder
Collagenopathy, types II and XI
Group of connective tissue conditions
Hereditary elliptocytosis
Genetic haematological condition