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.
Error occurred: cannot get document summary
*620788 - HIG1 HYPOXIA-INDUCIBLE DOMAIN FAMILY, MEMBER 2A; HIGD2A
Gene summaries Genetic tests Medical literature
#620784 - NEURODEVELOPMENTAL DISORDER PLUS OPTIC ATROPHY; NEDOA
#620783 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 115; DEE115
#620782 - NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT, AUTISM, AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER; NEDLAAD
#620780 - CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE ID; ARCL1D
*620778 - KILLER CELL IMMUNOGLOBULIN-LIKE RECEPTOR, THREE DOMAINS, SHORT CYTOPLASMIC TAIL, 1; KIR3DS1
#620777 - PULMONARY HYPERTENSION, PRIMARY, 6; PPH6
#620767 - SECKEL SYNDROME 11; SCKL11
*620766 - FORMATION OF MITOCHONDRIAL COMPLEX V ASSEMBLY FACTOR 1 HOMOLOG; FMC1
#620763 - CORNEAL DYSTROPHY, LISCH EPITHELIAL; LECD
*620751 - RETROTRANSPOSON GAG-LIKE 10; RTL10
*620749 - ZINC FINGER PROTEIN 438; ZNF438
#620748 - MEGALENCEPHALY-POLYDACTYLY SYNDROME; MPAPA
#620745 - DEAFNESS, AUTOSOMAL RECESSIVE 123; DFNB123
*620740 - STATHMIN 4; STMN4
#620732 - NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS, SEIZURES, AND STRUCTURAL BRAIN ABNORMALITIES; NEDMSB
#620731 - MICROPHTHALMIA/COLOBOMA 11; MCOPCB11
#620730 - HYPEREMESIS GRAVIDARUM, SUSCEPTIBILITY TO; HG
#620728 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1C; UCMD1C
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on