en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders
DiGeorge syndrome
A
Acropectoral syndrome
Acute intermittent porphyria
Adermatoglyphia
Albright's hereditary osteodystrophy
Arakawa's syndrome II
Aromatase excess syndrome
Autosomal dominant cerebellar ataxia
Axenfeld syndrome
B
Benign hereditary chorea
Bethlem myopathy
Birt–Hogg–Dubé syndrome
Boomerang dysplasia
Branchio-oto-renal syndrome
Buschke–Ollendorff syndrome
C
Camurati–Engelmann disease
Central core disease
Collagen disease
Collagenopathy, types II and XI
Congenital distal spinal muscular atrophy
Congenital stromal corneal dystrophy
Costello syndrome
Currarino syndrome
D
Darier's disease
De Vivo disease
Dentatorubral-pallidoluysian atrophy
Dermatopathia pigmentosa reticularis
Dysfibrinogenemia
F
Transthyretin-related hereditary amyloidosis
Familial atrial fibrillation
Familial hypercholesterolemia
Familial male-limited precocious puberty
Feingold syndrome
Felty's syndrome
Flynn–Aird syndrome
G
Gardner's syndrome
Gillespie syndrome
Gray platelet syndrome
Greig cephalopolysyndactyly syndrome
H
Hajdu–Cheney syndrome
Hawkinsinuria
Hay–Wells syndrome
Hereditary elliptocytosis
Hereditary hemorrhagic telangiectasia
Hereditary mucoepithelial dysplasia
Hereditary spherocytosis
Holt–Oram syndrome
Huntington's disease
Huntington's disease-like syndrome
Hypertrophic cardiomyopathy
Hypoalphalipoproteinemia
Hypochondroplasia
J
Jackson–Weiss syndrome
K
Keratolytic winter erythema
Kniest dysplasia
Kostmann syndrome
L
Langer–Giedion syndrome
Larsen syndrome
Liddle's syndrome
M
Marfan syndrome
Marshall syndrome
Medullary cystic kidney disease
Metachondromatosis
Miller–Dieker syndrome
MOMO syndrome
Monilethrix
Multiple endocrine neoplasia
Multiple endocrine neoplasia type 1
Multiple endocrine neoplasia type 2
Multiple endocrine neoplasia type 2b
Myelokathexis
Myotonic dystrophy
N
Naegeli–Franceschetti–Jadassohn syndrome
Nail–patella syndrome
Noonan syndrome
O
Oculopharyngeal muscular dystrophy
P
Pachyonychia congenita
Pallister–Hall syndrome
PAPA syndrome
Papillorenal syndrome
Parastremmatic dwarfism
Pelger–Huet anomaly
Peutz–Jeghers syndrome
Piebaldism
Platyspondylic lethal skeletal dysplasia, Torrance type
Polydactyly
Popliteal pterygium syndrome
Porphyria cutanea tarda
Pseudoachondroplasia
R
RASopathy
Reis–Bucklers corneal dystrophy
Romano–Ward syndrome
Rosselli–Gulienetti syndrome
Roussy–Lévy syndrome
Rubinstein–Taybi syndrome
S
Saethre–Chotzen syndrome
Schmitt Gillenwater Kelly syndrome
Short QT syndrome
Singleton Merten syndrome
Spinal muscular atrophy with lower extremity predominance
Spinocerebellar ataxia
Spinocerebellar ataxia type 6
Spondyloepimetaphyseal dysplasia, Strudwick type
Spondyloepiphyseal dysplasia congenita
Spondyloperipheral dysplasia
Stickler syndrome
T
Tietz syndrome
Timothy syndrome
Treacher Collins syndrome
Tuberous sclerosis
U
Upington disease
V
Variegate porphyria
Vitelliform macular dystrophy
Von Hippel–Lindau disease
Von Willebrand disease
W
Wallis–Zieff–Goldblatt syndrome
WHIM syndrome
White sponge nevus
Worth syndrome
Z
Zaspopathy
Zimmermann–Laband syndrome
Zori–Stalker–Williams syndrome