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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы
Найдено 1,772 заболеваний (Malform.) Сброс

SMARCA2-related blepharophimosis-intellectual disability syndrome

ORPHA:637013Malform.
Autosomal dominant

SPECC1L-related hypertelorism syndrome

ORPHA:1519Malform.
Autosomal dominant

STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome

ORPHA:502434Malform.
Autosomal dominant

Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome

ORPHA:397927Malform.
Autosomal recessive

Saethre-Chotzen syndrome

ORPHA:794Malform.
Autosomal dominant

Sanjad-Sakati syndrome

ORPHA:2323Malform.
Autosomal recessive

Say-Barber-Miller syndrome

ORPHA:3132Malform.
Unknown

Scalp defects-postaxial polydactyly syndrome

ORPHA:1003Malform.
Autosomal dominant

Scalp-ear-nipple syndrome

ORPHA:2036Malform.
Autosomal dominant

Schilbach-Rott syndrome

ORPHA:2353Malform.
Autosomal dominant

Schinzel-Giedion syndrome

ORPHA:798Malform.
Autosomal dominant, Not applicable

Schisis association

ORPHA:63862Malform.
Not applicable, Unknown

Schneckenbecken dysplasia

ORPHA:3144Malform.
Autosomal recessive

Schnitzler syndrome

ORPHA:37748Malform.
Not applicable

Schuurs-Hoeijmakers syndrome

ORPHA:329224Malform.
Autosomal dominant

Scimitar syndrome

ORPHA:185Malform.
Not applicable

Sclerosteosis

ORPHA:3152Malform.
Autosomal recessive

Seckel syndrome

ORPHA:808Malform.
Autosomal recessive

Segmental venous malformation

ORPHA:217008Malform.
Not applicable

Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome

ORPHA:659975Malform.
Autosomal recessive

Septo-optic dysplasia spectrum

ORPHA:3157Malform.
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, Not applicable

Severe X-linked intellectual disability, Gustavson type

ORPHA:3078Malform.
X-linked recessive

Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome

ORPHA:488627Malform.
Autosomal recessive

Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome

ORPHA:466688Malform.
Autosomal recessive