orphafolder

| 98602 | Rare disorder of the lacrimal apparatus
| 98605 | Lacrimal drainage system anomaly
| 98606 | Syndromic orbital border hypoplasia
| 98604 | Congenital alacrima
| 98594 | Rare eyebrow/eyelash disorder
| 98593 | Neurogenic palpebral tumor
| 98592 | Palpebral tumor with a vascular malformation
| 98591 | Mesenchymatous palpebral tumor
| 98586 | Pigmented palpebral tumor
| 98585 | Palpebral sebaceous gland tumor
| 98584 | Malignant tumor of palpebral epidermis
| 98583 | Precancerous lesion of palpebral epidermis
| 98590 | Palpebral piliary tumor
| 98588 | Palpebral nevus
| 98587 | Palpebral lentiginosis
| 98575 | Syndromic telecanthus
| 98576 | Syndromic outer canthal malposition
| 98578 | Rare disorder with ptosis
| 98580 | Palpebral tumor
| 98581 | Palpebral epidermal tumor
| 98582 | Benign tumor of palpebral epidermis
| 98567 | Rare eyelid malposition disorder
| 98570 | Congenital ectropion
| 98571 | Secondary ectropion
| 98574 | Syndromic epicanthus
| 98560 | Rare palpebral disorder
| 98562 | Cryptophthalmia
| 98561 | Congenital malformation of the eyelid
| 98564 | Eyelid border anomaly
| 98563 | Microblepharon-ablephara syndrome
| 98566 | Syndromic eyelid coloboma
| 98565 | Syndromic ankyloblepharon filiforme adnatum
| 98553 | Developmental defect of the eye
| 98555 | Microphthalmia-anophthalmia-coloboma
| 98557 | Syndromic aniridia
| 98676 | Autosomal recessive isolated optic atrophy
| 98673 | Autosomal dominant optic atrophy, classic form
| 98671 | Hereditary optic neuropathy
| 98672 | Autosomal dominant optic atrophy
| 98668 | Vitreoretinopathy
| 98661 | Syndromic rod-cone dystrophy
| 98658 | Color-vision disease
| 98655 | Lens shape anomaly
| 98653 | Lens position anomaly
| 98652 | Lens size anomaly
| 98650 | Craniofacial anomaly with cataract
| 98649 | Dentocutaneous disease with cataract
| 98648 | Musculoskeletal disease with cataract
| 98644 | Metabolic disease with cataract
| 98646 | Renal disease with cataract
| 98639 | Rare lens disease
| 98640 | Rare disorder with lens opacification
| 98641 | Syndromic cataract
| 98642 | Chromosomal anomaly with cataract
| 98635 | Corneodysgenesis
| 98638 | Rare disease with glaucoma as a major feature
| 98631 | Congenital malformation of the eye with glaucoma as a major feature
| 98634 | Anterior segment developmental anomaly without extraocular manifestation
| 98628 | Syndromic corneal dystrophy
| 98627 | Posterior corneal dystrophy
| 98623 | Syndromic keratoconus
| 98626 | Stromal corneal dystrophy
| 98625 | Superficial corneal dystrophy
| 98619 | Rare isolated myopia
| 98622 | Syndromic hyperopia
| 98621 | Rare hyperopia and astigmatism
| 98618 | Rare refraction anomaly
| 98729 | Congenital pulmonary veins anomaly
| 98727 | Rare atrial defect and interatrial communication
| 98733 | Noonan syndrome and Noonan-related syndrome
| 98731 | Congenital arteriovenous fistula
| 98738 | Neurological muscular channelopathy due to a genetic sodium channel defect
| 98737 | Genetic neurological muscular channelopathy
| 98736 | Genetic neurological channelopathy
| 98742 | Neurological muscular channelopathy due to a genetic ryanodine receptor defect
| 98741 | Neurological muscular channelopathy due to a genetic potassium channel defect
| 98740 | Neurological muscular channelopathy due to a genetic calcium channel defect
| 98739 | Neurological muscular channelopathy due to a genetic chloride channel defect
| 98717 | Transposition of the great arteries and conotruncal cardiac anomaly
| 98718 | Aortic malformation
| 98715 | Uveitis
| 98716 | Heart position anomaly
| 98721 | Congenital tricuspid malformation
| 98722 | Atrioventricular canal defect
| 98719 | Pulmonary artery or pulmonary branch anomaly
| 98720 | Atrioventricular valve anomaly
| 98725 | Ascending aorta anomaly
| 98723 | Hypoplastic right heart syndrome
| 98724 | Congenital anomaly of the great arteries
| 98706 | Oculocutaneous or ocular albinism
| 98681 | Rare disorder with strabismus
| 98683 | Syndromic disorder with strabismus
| 98684 | Craniostenosis with strabismus
| 98685 | Rare oculomotor nerve disorder
| 98686 | Congenital trochlear nerve palsy
| 98687 | Supranuclear eye movement disorder
| 98688 | Oculomotor apraxia
| 98798 | Isochromosomy Yq
| 98797 | Isochromosomy Yp
| 98795 | Angelman syndrome due to paternal uniparental disomy of chromosome 15

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