MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
1,772 Erkrankungen gefunden (Malf.) Zurücksetzen

SMARCA2-related blepharophimosis-intellectual disability syndrome

ORPHA:637013Malf.
Autosomal dominant

SPECC1L-related hypertelorism syndrome

ORPHA:1519Malf.
Autosomal dominant

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

ORPHA:502434Malf.
Autosomal dominant

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

ORPHA:397927Malf.
Autosomal recessive

Saethre-Chotzen syndrome

ORPHA:794Malf.
Autosomal dominant

Sanjad-Sakati syndrome

ORPHA:2323Malf.
Autosomal recessive

Say-Barber-Miller syndrome

ORPHA:3132Malf.
Unknown

Scalp defects-postaxial polydactyly syndrome

ORPHA:1003Malf.
Autosomal dominant

Scalp-ear-nipple syndrome

ORPHA:2036Malf.
Autosomal dominant

Schilbach-Rott syndrome

ORPHA:2353Malf.
Autosomal dominant

Schinzel-Giedion syndrome

ORPHA:798Malf.
Autosomal dominant, Not applicable

Schisis association

ORPHA:63862Malf.
Not applicable, Unknown

Schneckenbecken dysplasia

ORPHA:3144Malf.
Autosomal recessive

Schnitzler syndrome

ORPHA:37748Malf.
Not applicable

Schuurs-Hoeijmakers syndrome

ORPHA:329224Malf.
Autosomal dominant

Scimitar syndrome

ORPHA:185Malf.
Not applicable

Sclerosteosis

ORPHA:3152Malf.
Autosomal recessive

Seckel syndrome

ORPHA:808Malf.
Autosomal recessive

Segmental venous malformation

ORPHA:217008Malf.
Not applicable

Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome

ORPHA:659975Malf.
Autosomal recessive

Septo-optic dysplasia spectrum

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

Severe X-linked intellectual disability, Gustavson type

ORPHA:3078Malf.
X-linked recessive

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

ORPHA:488627Malf.
Autosomal recessive

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

ORPHA:466688Malf.
Autosomal recessive