SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Description of facility

Director / Spokesperson
Dr. Dirk Biskup, Dr. Dr. Saskia Biskup
Information
Care facility for adults and children
Description
Als mittelständischer Dienstleister im Bereich der Medizin und Biotechnologie wird hier die Entschlüsselung von Erbinformationen und die medizinische Interpretation der Daten angeboten.

Consultation hours

nach Vereinbarung.

Care provisions

This facility offers the following
  • Genetic counselling
  • Clinical studies / research
  • Diagnostic

Contact

Information
07071 5654455
07071 5654456
info@cegat.de
Website https://www.cegat.de/

Address

Paul-Ehrlich-Straße 23
72076 Tübingen

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Preview of the assigned diseases 4

Pfeiffer syndrome Cockayne syndrome type 2 Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Cockayne syndrome type 1 Cockayne syndrome type 3 Antenatal Bartter syndrome Bartter syndrome type 3 Infantile spasms syndrome Angelman syndrome due to paternal uniparental disomy of chromosome 15 Angelman syndrome due to maternal 15q11q13 deletion Bohring-Opitz syndrome Bartter syndrome with hypocalcemia Fabry disease Cockayne syndrome Bartter syndrome type 4 Leigh syndrome with leukodystrophy Hypopituitarism-postaxial polydactyly syndrome Alport syndrome Leigh syndrome with nephrotic syndrome Crouzon syndrome Angelman syndrome Muenke syndrome Antley-Bixler syndrome Fanconi anemia Keratoderma hereditarium mutilans Wilson disease Stickler syndrome type 2 Stickler syndrome type 1 Lafora disease Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type Rett syndrome Duane retraction syndrome Leigh syndrome with cardiomyopathy Leigh syndrome Pfeiffer syndrome type 1 COFS syndrome Dursun syndrome Pfeiffer syndrome type 3 Pfeiffer syndrome type 2 Greig cephalopolysyndactyly syndrome Retinitis pigmentosa Partington syndrome Bardet-Biedl syndrome Bartter syndrome X-linked Alport syndrome Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome CHARGE syndrome Usher syndrome type 3 Stargardt disease Stickler syndrome Becker muscular dystrophy Duchenne muscular dystrophy Meckel syndrome Autosomal recessive Stickler syndrome Angelman syndrome due to imprinting defect in 15q11-q13 Angelman syndrome due to a point mutation
9.05513848.5381605CeGaT GmbH
Last updated: 25.10.2022