Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Lissencephaly with cerebellar hypoplasia
Lissencephaly with cerebellar hypoplasia type A
Antenatal, Neonatal
Lissencephaly with cerebellar hypoplasia type B
Antenatal, Infancy, Neonatal
Lissencephaly with cerebellar hypoplasia type C
Neonatal
Lissencephaly with cerebellar hypoplasia type D
Antenatal, Neonatal
Lissencephaly with cerebellar hypoplasia type E
Antenatal, Neonatal
Lissencephaly with cerebellar hypoplasia type F
Antenatal, Neonatal
Listeriosis
Not applicable
All ages
Livedoid vasculopathy
Adolescent, Adult
Liver adenomatosis
Adult, Elderly
Lobar holoprosencephaly
Multigenic/multifactorial, Not applicable
Infancy, Neonatal
Localized dystrophic epidermolysis bullosa
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Localized dystrophic epidermolysis bullosa, acral form
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Localized dystrophic epidermolysis bullosa, nails only
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Localized dystrophic epidermolysis bullosa, pretibial form
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Localized epidermolysis bullosa simplex
Autosomal dominant
Childhood
Localized junctional epidermolysis bullosa
Autosomal recessive
Infancy, Neonatal
Localized lichen myxedematosus with mixed features of different subtypes
Adult, Elderly
Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms
Adult, Elderly
Localized lipodystrophy
Unknown
All ages
Localized pagetoid reticulosis
Not applicable
Adult
Localized scleroderma
Not applicable
All ages
Locked-in syndrome
Not applicable
All ages
Loeffler endocarditis
Adolescent, Adult, Childhood