Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
#208050 - ARTERIAL TORTUOSITY SYNDROME; ATORS
Cytogenetic locations: associated
Gene summaries Genetic tests Medical literature
#620056 - POLYCYSTIC KIDNEY DISEASE 7; PKD7
Cytogenetic locations: 12q24.31
#620780 - CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE ID; ARCL1D
#603041 - MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1
Cytogenetic locations: 12725645
#615349 - EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2
Cytogenetic locations: 1p36.33
%151900 - LIPOMATOSIS, FAMILIAL MULTIPLE; FML
#606408 - EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 1; EDSCLL1
Cytogenetic locations: 6p21.33
#173900 - POLYCYSTIC KIDNEY DISEASE 1 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD1
Cytogenetic locations: 16127487
221400 - DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL AND PROGRESSIVE SENSORY NEUROPATHY
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on