MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Spondyloepiphyseal dysplasia, Stanescu type

ORPHA:459051Kr.
Autosomal dominant

Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome

ORPHA:163654Kr.
Unknown

Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome

ORPHA:163649Kr.
Autosomal recessive

Spondylometaphyseal dysplasia

ORPHA:254Kl. gruppe
Autosomal dominant, Autosomal recessive, X-linked recessive

Spondylometaphyseal dysplasia, 'corner fracture' type

ORPHA:93315Kr.
Autosomal dominant

Spondylometaphyseal dysplasia, A4 type

ORPHA:168555Kr.
Autosomal recessive

Spondylometaphyseal dysplasia, Golden type

ORPHA:168544Kr.
X-linked recessive

Spondylometaphyseal dysplasia, Kozlowski type

ORPHA:93314Kr.
Autosomal dominant

Spondylometaphyseal dysplasia, Schmidt type

ORPHA:93316Kr.
Autosomal dominant

Spondylometaphyseal dysplasia, Sedaghatian type

ORPHA:93317Malf.
Autosomal recessive

Spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome

ORPHA:168552Kr.
Autosomal recessive

Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome

ORPHA:85167Kr.
Autosomal recessive

Spondylometaphyseal dysplasia-corneal dystrophy syndrome

ORPHA:589435Malf.
Autosomal recessive

Spondyloperipheral dysplasia-short ulna syndrome

ORPHA:1856Kr.
Autosomal dominant

Spontaneous intracranial hypotension

ORPHA:443180Kr.
Not applicable

Spontaneous periodic hypothermia

ORPHA:29822Kr.
Unknown

Sporadic Creutzfeldt-Jakob disease

ORPHA:204Kr.
Not applicable

Sporadic adult-onset ataxia of unknown etiology

ORPHA:247234Kr.
Not applicable

Sporadic fatal insomnia

ORPHA:586130Kr.

Sporadic fetal brain disruption sequence

ORPHA:1665Malf.
Not applicable

Sporadic infantile bilateral striatal necrosis

ORPHA:225147Kr.
Not applicable

Sporadic pheochromocytoma/secreting paraganglioma

ORPHA:276621Kr.
Not applicable

Sporadic porphyria cutanea tarda

ORPHA:443057Kl. subt.
Multigenic/multifactorial

Sporotrichosis

ORPHA:826Kr.
Not applicable