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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Lewis-Sumner syndrome

ORPHA:48162Клин. подт.
Not applicable

Leydig cell hypoplasia

ORPHA:755Заболевание

Leydig cell hypoplasia due to LHB deficiency

ORPHA:325448Клин. подт.
Autosomal recessive

Leydig cell hypoplasia due to complete LH resistance

ORPHA:96265Клин. подт.
Autosomal recessive

Leydig cell hypoplasia due to partial LH resistance

ORPHA:96266Клин. подт.
Autosomal recessive

Lhermitte-Duclos disease

ORPHA:65285Клин. подт.
Autosomal dominant, Not applicable

Li-Fraumeni syndrome

ORPHA:524Заболевание
Autosomal dominant

Lichen amyloidosis

ORPHA:49804Заболевание

Lichen myxedematosus

ORPHA:402007Клин. гр.

Lichen planopilaris

ORPHA:525Заболевание
Not applicable

Lichen planus pemphigoides

ORPHA:254478Заболевание

Lichen planus pigmentosus

ORPHA:254463Заболевание

Lichtenstein syndrome

ORPHA:2390Заболевание
Autosomal recessive

Liddle syndrome

ORPHA:526Заболевание
Autosomal dominant

Limb body wall complex

ORPHA:2369Порок
Not applicable

Limb-girdle muscular dystrophy

ORPHA:263Клин. гр.
Autosomal dominant, Autosomal recessive

Limb-girdle muscular dystrophy due to POMK deficiency

ORPHA:445110Заболевание
Autosomal recessive

Limb-mammary syndrome

ORPHA:69085Порок
Autosomal dominant

Limbal stem cell deficiency

ORPHA:171673Заболевание
Not applicable

Limited cutaneous systemic sclerosis

ORPHA:220402Клин. подт.
Multigenic/multifactorial, Not applicable

Limited systemic sclerosis

ORPHA:220407Клин. подт.
Not applicable

Linear IgA dermatosis

ORPHA:46488Заболевание
Not applicable

Linear and whorled nevoid hypermelanosis

ORPHA:79150Заболевание

Linear atrophoderma of Moulin

ORPHA:140933Заболевание