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.
#620292 - NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES; NEDLBAS
Cytogenetic locations: p#####
Gene summaries Genetic tests Medical literature
#620193 - LACRIMOAURICULODENTODIGITAL SYNDROME 3; LADD3
Cytogenetic locations: 617233
#620192 - LACRIMOAURICULODENTODIGITAL SYNDROME 2; LADD2
#620071 - BIRK-AHARONI SYNDROME; BKAH
Cytogenetic locations: #1q}##
#620038 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND ABSENT LANGUAGE; NEDMHAL
#620019 - ARTHROGRYPOSIS, DISTAL, TYPE 11; DA11
Cytogenetic locations: #n{###
#619947 - WAARDENBURG SYNDROME, TYPE 2F; WS2F
Cytogenetic locations: 0,#_##
#619652 - IMMUNODEFICIENCY 92; IMD92
Cytogenetic locations: ###X##
#619538 - CEREBRAL CAVERNOUS MALFORMATIONS 4; CCM4
#619465 - VISCERAL NEUROPATHY, FAMILIAL, 2, AUTOSOMAL RECESSIVE; VSCN2
Cytogenetic locations: ######
#619354 - DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP
Cytogenetic locations: assignment
#619339 - BARTSOCAS-PAPAS SYNDROME 2; BPS2
Cytogenetic locations: 138250
#619281 - IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE; IMD14B
Cytogenetic locations: 1p36.22
#619243 - GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES; GDSBA
#619175 - PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 5; PRAAS5
Cytogenetic locations: 0#w\##
#619149 - LESSEL-KREIENKAMP SYNDROME; LESKRES
Cytogenetic locations: ##k###
#619087 - NOONAN SYNDROME 13; NS13
Cytogenetic locations: 0#{}##
#618914 - NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME; NEDJED
#618858 - DIABETES MELLITUS, PERMANENT NEONATAL, 4; PNDM4
Cytogenetic locations: 11p15.5
#618681 - LESSEL-KUBISCH SYNDROME; LSKB
Cytogenetic locations: #d####
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on