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.
#620731 - MICROPHTHALMIA/COLOBOMA 11; MCOPCB11
Gene summaries Genetic tests Medical literature
#620654 - THROMBOCYTOPENIA 11 WITH MULTIPLE CONGENITAL ANOMALIES AND DYSMORPHIC FACIES; THC11
#620558 - CRANIOMETADIAPHYSEAL OSTEOSCLEROSIS WITH HIP DYSPLASIA; CMDOH
Cytogenetic locations: Kif7
#620514 - IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION; IDAA
Cytogenetic locations: `#####
#620512 - SPASTIC PARAPLEGIA 18A, AUTOSOMAL DOMINANT; SPG18A
Cytogenetic locations: P#####
#620457 - AURICULOCONDYLAR SYNDROME 4; ARCND4
Cytogenetic locations: #J"###
#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{###
#620012 - DEVELOPMENTAL DELAY, HYPOTONIA, AND IMPAIRED LANGUAGE; DEDHIL
#619947 - WAARDENBURG SYNDROME, TYPE 2F; WS2F
Cytogenetic locations: 0,#_##
#619797 - NEURODEVELOPMENTAL DISORDER WITH CENTRAL HYPOTONIA AND DYSMORPHIC FACIES; NEDCHF
Cytogenetic locations: #e####
#619793 - RESTRICTIVE DERMOPATHY 2; RSDM2
Cytogenetic locations: mutation
#619657 - CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 8, WITH OR WITHOUT HETEROTAXY; CHTD8
Cytogenetic locations: pb#x##
#619656 - LOEYS-DIETZ SYNDROME 6; LDS6
Cytogenetic locations: 0^#d##
*619640 - LYSINE DEMETHYLASE 7A; KDM7A
Cytogenetic locations: -
#619574 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2HH; CMT2HH
Cytogenetic locations: 605234
#619566 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 27; LGMDR27
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on