Mapping of Health Care Providers
for People with Rare Diseases

Decription of facility

Director / Spokesperson
Dr. Dirk Biskup; Dr. Dr. Saskia Biskup
Care facility for adults and children

Als mittelständischer Dienstleister im Bereich der Medizin und Biotechnologie bieten sie die Entschlüsselung von Erbinformationen und die medizinische Interpretation der Daten an.

Consultation hours

Special consultation hours:
Nach Vereinbarung.

Care provisions

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


07071 5654455
07071 5654456


Paul-Ehrlich-Straße 23
72076 Tübingen

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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 Classic Bartter syndrome West 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 Infantile Bartter syndrome with sensorineural deafness Leigh syndrome with leukodystrophy Kein Name gefunden Alport syndrome Leigh syndrome with nephrotic syndrome Crouzon disease 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

Provided care options 0

No available care options have been entered.
9.05794961694944748.538301170118565CeGaT GmbH
Last updated: 18.12.2019