Additional Disease Briefs

epileptic encephalopathy, infantile or early childhood, 3

Also known as: IECEE3, developmental and epileptic encephalopathy 93, epileptic encephalopathy, infantile or early childhood, 3

epiphyseal dysplasia-hearing loss-dysmorphism syndrome

Also known as: Finucane Kurtz Scott syndrome, Finucane-Kurtz-Scott syndrome, epiphyseal dysplasia hearing loss dysmorphism

epiphyseal dysplasia, multiple, 2

Also known as: COL9A2 multiple epiphyseal dysplasia (disease), EDM2, epiphyseal dysplasia multiple 2, epiphyseal dysplasia, multiple, 2, epiphyseal dysplasia, multiple, type 2, multiple epiphyseal dysplasia (disease) caused by mutation in COL9A2, multiple epiphyseal dysplasia 2

epiphyseal dysplasia, multiple, 3

Also known as: COL9A3 multiple epiphyseal dysplasia (disease), EDM3, epiphyseal dysplasia multiple 3, epiphyseal dysplasia, multiple, 3, epiphyseal dysplasia, multiple, 3, with myopathy, epiphyseal dysplasia, multiple, 3, with or without myopathy, epiphyseal dysplasia, multiple, type 3, multiple epiphyseal dysplasia (disease) caused by mutation in COL9A3, multiple epiphyseal dysplasia 3

epiphyseal dysplasia, multiple, 6

Also known as: COL9A1 multiple epiphyseal dysplasia (disease), EDM6, epiphyseal dysplasia, multiple, 6, epiphyseal dysplasia, multiple, type 6, multiple epiphyseal dysplasia (disease) caused by mutation in COL9A1, multiple epiphyseal dysplasia 6

epiphyseal dysplasia, multiple, 7

Also known as: EDM7, epiphyseal dysplasia, multiple, 7, multiple epiphyseal dysplasia 7, multiple epiphyseal dysplasia type 7

epiphysiolysis of the hip

Also known as: SCFE, SUFE, SufE, epiphysiolysis capitis femoris, epiphysiolysis of the upper femur, femoral head epiphysiolysis, slipped capital femoral epiphysis, slipped femoral capital epiphyses, slipped upper femoral epiphysis

episodic angioedema with eosinophilia

Also known as: EAE, Gleich syndrome, Gleich's syndrome

episodic ataxia type 1

Also known as: EA1, Isaacs-Mertens syndrome, KCNA1 hereditary episodic ataxia, acetazolamide-responsive periodic ataxia, ataxia, episodic, with myokymia, continuous muscle fiber activity, continuous muscle fiber activity, hereditary, continuous muscle fibre activity, continuous muscle fibre activity, hereditary, episodic ataxia with myokymia, episodic ataxia, type 1, episodic ataxia/myokymia syndrome, familial paroxysmal kinesigenic ataxia and continuous myokymia, hereditary episodic ataxia caused by mutation in KCNA1, hereditary paroxysmal ataxia with neuromyotonia, myokymia 1, myokymia 1 with or without hypomagnesemia, myokymia with periodic ataxia, paroxysmal ataxia with neuromyotonia, hereditary

episodic ataxia type 2