Genetic dermis disorder
ORPHA:183472Genetic dermis elastic tissue disorder
ORPHA:228215Genetic difference of sex development
ORPHA:325690Genetic epidermal disorder
ORPHA:183426Genetic mixed dermis disorder
ORPHA:183481Genetic primary orthostatic disorder
ORPHA:521232Genetic skin vascular disorder
ORPHA:183478Genetic subcutaneous tissue disorder
ORPHA:183484OBSOLETE: Rare genetic choroidal disorder
ORPHA:522584Other genetic dermis disorder
ORPHA:477808Rare choreic movement disorder
ORPHA:306715Rare choroidal disorder
ORPHA:519309Rare corneal disorder
ORPHA:519282Rare disorder of the pupil
ORPHA:519286Rare disorder with ptosis
ORPHA:98578Rare dystonia
ORPHA:68363Rare eyebrow/eyelash disorder
ORPHA:98594Rare genetic adrenal disease
ORPHA:183637Rare genetic autonomic nervous system disorder
ORPHA:434786Rare genetic bone development disorder
ORPHA:404584Rare genetic bone disease
ORPHA:183524Rare genetic cardiac disease
ORPHA:98054Rare genetic coagulation disorder
ORPHA:183654Rare genetic corneal disorder
ORPHA:522556Rare genetic deafness
ORPHA:96210Rare genetic diabetes mellitus
ORPHA:183625Rare genetic disease
ORPHA:98053Rare genetic disorder of the anterior segment of the eye
ORPHA:522538Rare genetic disorder of the lacrimal apparatus
ORPHA:522532Rare genetic disorder of the ocular adnexa
ORPHA:522524Rare genetic disorder of the posterior segment of the eye
ORPHA:522570Rare genetic disorder of the pupil
ORPHA:522568Rare genetic disorder of the visual organs
ORPHA:522504Rare genetic disorder with entropion
ORPHA:522530Rare genetic disorder with lens opacification
ORPHA:522546Rare genetic disorder with obstructive azoospermia
ORPHA:400003Rare genetic disorder with strabismus
ORPHA:522518Rare genetic dystonia
ORPHA:391799Rare genetic endocrine disease
ORPHA:156638Rare genetic epilepsy
ORPHA:183512Rare genetic eye disease
ORPHA:101435Rare genetic eyelid malposition disorder
ORPHA:522528Rare genetic headache
ORPHA:183509Rare genetic hematologic disease
ORPHA:158300Rare genetic hepatic disease
ORPHA:156601Rare genetic hyperkinetic movement disorder
ORPHA:496916Rare genetic immune disease
ORPHA:183770Rare genetic inflammatory/autoimmune corneal disorder
ORPHA:522566