orphafolder

| 49042 | Dentinogenesis imperfecta
| 48431 | Congenital cataracts-facial dysmorphism-neuropathy syndrome
| 48471 | Lissencephaly
| 48435 | Postinfectious vasculitis
| 48686 | Primary effusion lymphoma
| 48652 | Monosomy 22q13
| 50809 | Talo-patello-scaphoid osteolysis
| 50810 | Microlissencephaly-micromelia syndrome
| 50811 | Lipodystrophy-intellectual disability-deafness syndrome
| 50812 | Zellweger-like syndrome without peroxisomal anomalies
| 50814 | Craniolenticulosutural dysplasia
| 50815 | Branchiogenic deafness syndrome
| 50816 | Spondylometaphyseal dysplasia with combined immunodeficiency
| 49566 | Acquired purpura fulminans
| 49804 | Lichen amyloidosis
| 49827 | Thiamine-responsive megaloblastic anemia syndrome
| 50251 | Pleural mesothelioma
| 50945 | Blomstrand lethal chondrodysplasia
| 50944 | Schöpf-Schulz-Passarge syndrome
| 51084 | Torsade-de-pointes syndrome with short coupling interval
| 51083 | Familial short QT syndrome
| 50839 | Cat-scratch disease
| 50817 | Duane anomaly-myopathy-scoliosis syndrome
| 50943 | Keratolytic winter erythema
| 50942 | Striate palmoplantar keratoderma
| 50920 | Multiple fibroadenoma of the breast
| 50918 | Kikuchi-Fujimoto disease
| 52054 | Craniosynostosis-intracranial calcifications syndrome
| 52022 | Potocki-Shaffer syndrome
| 52047 | Braddock syndrome
| 51577 | Cobblestone lissencephaly
| 51608 | Generalized arterial calcification of infancy
| 51188 | Ethylmalonic encephalopathy
| 51208 | Formiminoglutamic aciduria
| 51636 | WHIM syndrome
| 51890 | Anterior cutaneous nerve entrapment syndrome
| 68419 | Vascular anomaly or angioma
| 42642 | PFAPA syndrome
| 42665 | Tietz syndrome
| 43117 | Acute tricyclic antidepressant poisoning
| 43116 | Serotonin syndrome
| 43393 | Lambert-Eaton myasthenic syndrome
| 43119 | Acute poisoning by drugs with membrane-stabilizing effect
| 42775 | PHACE syndrome
| 42738 | Severe congenital neutropenia
| 43115 | Hereditary myopathy with lactic acidosis due to ISCU deficiency
| 45448 | Miyoshi myopathy
| 45453 | Incessant infant ventricular tachycardia
| 45452 | Idiopathic neonatal atrial flutter
| 44890 | Gastrointestinal stromal tumor
| 45358 | Congenital fibrosis of extraocular muscles
| 46487 | Acquired epidermolysis bullosa
| 46488 | Linear IgA dermatosis
| 46485 | Superficial pemphigus
| 46486 | Mucous membrane pemphigoid
| 46348 | Paroxysmal extreme pain disorder
| 46484 | Oligodendroglial tumor
| 46059 | Lathosterolosis
| 46135 | Primary central nervous system lymphoma
| 47044 | Hereditary papillary renal cell carcinoma
| 46724 | Cerebral arteriovenous malformation
| 46627 | Char syndrome
| 46658 | Primordial short stature-microdontia-opalescent and rootless teeth syndrome
| 46532 | Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
| 48372 | Nodular regenerative hyperplasia of the liver
| 48162 | Lewis-Sumner syndrome
| 48104 | Pyoderma gangrenosum
| 47612 | Felty syndrome
| 47159 | Proximal renal tubular acidosis
| 47045 | Familial cold urticaria
| 48377 | Subcorneal pustular dermatosis
| 68361 | Rare deafness
| 68362 | Rare vascular disease
| 68363 | Rare dystonia
| 68364 | Hemoglobinopathy
| 68366 | Lysosomal disease
| 68367 | Rare inborn errors of metabolism
| 68373 | Peroxisomal disease
| 68378 | Congenital limb malformation
| 68381 | Neuromuscular disease
| 68380 | Mitochondrial disease
| 68383 | Rare constitutional aplastic anemia
| 68385 | Neurometabolic disease
| 68402 | Rare parkinsonian disorder
| 68411 | Rare bone tumor
| 68416 | Rare infectious disease
| 68415 | Rare parathyroid disease and phosphocalcic metabolism anomaly
| 90065 | Acquired aneurysmal subarachnoid hemorrhage
| 90066 | Pneumonia caused by Pseudomonas aeruginosa infection
| 90068 | Cocaine intoxication
| 90061 | Non-infectious posterior uveitis
| 90062 | Acute liver failure
| 90064 | Acute peripheral arterial occlusion
| 90073 | Hepatitis B reinfection following liver transplantation
| 90076 | Partial deep dermal and full thickness burns
| 90069 | Systemic monochloroacetate poisoning
| 90050 | Retinopathy of prematurity
| 90045 | Hereditary folate malabsorption
| 90052 | Recurrent hepatitis C virus induced liver disease in liver transplant recipients
| 90051 | Sepsis in premature infants

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