Terminology Service for NFDI4Health
autosomal dominant inheritance
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http://purl.obolibrary.org/obo/GENO_0000147
An inheritance pattern wherein a trait caused by alleles of an autosomal gene manifests to some degree in heterozygotes.
Term info
Label
autosomal dominant inheritance
Term relations
Related from:
has material basis in
- LEOPARD syndrome
- Muckle-Wells syndrome
- familial encephalopathy with neuroserpin inclusion bodies
- Townes-Brocks syndrome
- Koolen de Vries syndrome
- ichthyosis vulgaris
- rippling muscle disease 2
- autosomal dominant chondrodysplasia punctata
- autosomal dominant hypophosphatemic rickets
- Rapp-Hodgkin syndrome
- autosomal dominant sideroblastic anemia 4
- autosomal dominant non-syndromic intellectual disability
- cherubism
- punctate palmoplantar keratoderma type III
- Parkinson's disease 1
- Parkinson's disease 8
- microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
- Kleefstra syndrome 1
- acrofacial dysostosis Cincinnati type
- Stormorken syndrome
- hereditary multiple exostoses
- chromosome 13q14 deletion syndrome
- chromosome 15q11.2 deletion syndrome
- chromosome 15q24 deletion syndrome
- chromosome 15q25 deletion syndrome
- ADULT syndrome
- acrokeratosis verruciformis
- hereditary spastic paraplegia 72
- hereditary spastic paraplegia 73
- hereditary spastic paraplegia 6
- hereditary spastic paraplegia 8
- retinitis pigmentosa-deafness syndrome
- Rubinstein-Taybi syndrome
- Bannayan-Riley-Ruvalcaba syndrome
- Bart-Pumphrey syndrome
- advanced sleep phase syndrome
- Finnish type amyloidosis
- transthyretin amyloidosis
- brachydactyly-syndactyly syndrome
- Brooke-Spiegler syndrome
- branchiooculofacial syndrome
- Beare-Stevenson cutis gyrata syndrome
- inflammatory bowel disease 3
- Blau syndrome
- Birk-Barel syndrome
- Birt-Hogg-Dube syndrome
- holoprosencephaly 5
- holoprosencephaly 9
- holoprosencephaly 2
- holoprosencephaly 3
- holoprosencephaly 11
- holoprosencephaly 7
- popliteal pterygium syndrome
- holoprosencephaly 1
- holoprosencephaly 4
- posterior polymorphous corneal dystrophy 2
- posterior polymorphous corneal dystrophy 1
- congenital stationary night blindness autosomal dominant 1
- congenital stationary night blindness autosomal dominant 2
- brachydactyly type A2
- brachydactyly type A1
- nemaline myopathy 6
- autosomal dominant osteopetrosis 2
- autosomal dominant osteopetrosis 1
- nemaline myopathy 4
- hereditary spherocytosis type 4
- hereditary spherocytosis type 1
- hereditary spherocytosis type 2
- nemaline myopathy 1
- paraganglioma
- polycystic liver disease
- inflammatory bowel disease 21
- tarsal-carpal coalition syndrome
- juvenile polyposis syndrome
- proximal symphalangism
- iridogoniodysgenesis syndrome
- multiple cutaneous and mucosal venous malformations
- Timothy syndrome
- brachydactyly type C
- brachydactyly type D
- Lynch syndrome
- hereditary hemorrhagic telangiectasia
- pachyonychia congenita
- congenital myasthenic syndrome 4A
- congenital myasthenic syndrome 18
- congenital myasthenic syndrome 2A
- Hailey-Hailey disease
- congenital myasthenic syndrome 7
- long QT syndrome 10
- long QT syndrome 9
- long QT syndrome 12
- long QT syndrome 11
- long QT syndrome 14
- long QT syndrome 13
- long QT syndrome 15
- Frasier syndrome
- Andersen-Tawil syndrome
- congenital myasthenic syndrome 1B
- congenital myasthenic syndrome 1A