Additional Disease Briefs

congenital myotonic dystrophy

Also known as: Congenital Myotonic dystrophies, Congenital Myotonic dystrophy, Congenital myotonic dystrophy, MYOTONIC dystrophy CONGEN, Myotonic dystrophies, Congenital, Myotonic dystrophy, Congenital, congenital myotonic dystrophy, dystrophies, Congenital Myotonic, dystrophy, Congenital Myotonic

congenital narrowing of cervical spinal canal

Also known as: congenital cervical spinal stenosis, congenital stenosis of the cervical spine

congenital nephrotic syndrome, Finnish type

Also known as: CnF, Finnish congenital nephrosis, NPHS1, congenital nephrotic syndrome - Finnish type, congenital nephrotic syndrome 1, congenital nephrotic syndrome Finnish type, congenital nephrotic syndrome, Finnish type, nephrosis 1, congenital, Finnish type, nephrosis, congenital, nephrotic syndrome - NPHS1 associated, nephrotic syndrome, congenital, nephrotic syndrome, type 1

congenital neutropenia-myelofibrosis-nephromegaly syndrome

Also known as: SCN5, congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome, neutropenia, severe congenital, 5, autosomal recessive, vps45 deficiency

congenital non-bullous ichthyosiform erythroderma

Also known as: CIE, alligator skin, congenital ichthyosiform erythroderma, congenital ichthyosiform erythroderma (disease), congenital non bullous ichthyosiform erythroderma, erythrodermic ichthyosis, ichthyosiform erythroderma, lamellar desquamation of the newborn, lamellar ichthyosis, non-bullous congenital ichthyosiform erythroderma, nonbullous congenital ichthyosiform erythroderma

congenital non-communicating hydrocephalus

Also known as: congenital obstructive hydrocephalus

congenital nongoitrous hypothryoidism 3

Also known as: CHNG3, congenital nongoitrous hypothyroidism 3, hypothyroidism, congenital, nongoitrous, 3, resistance to thyrotropin, thyrotropin resistance

congenital nongoitrous hypothryoidism 6

Also known as: CHNG6, THRA hypothyroidism, congenital, nongoitrous, congenital nongoitrous hypothyroidism 6, hypothyroidism, congenital, nongoitrous caused by mutation in THRA, hypothyroidism, congenital, nongoitrous, 6, hypothyroidism, congenital, nongoitrous, type 6

congenital oculomotor nerve palsy

Also known as: congenital CNIII lesion, congenital third cranial nerve palsy

congenital or early infantile CACH syndrome