I Cell Disease
Also known as: GNPTA Inclusion Cell Disease Leroy Disease ML Disorder, Type II ML II Mucolipidosis II N-Acetylglucosamine-1-Phosphotransferase Deficiency
Also known as: GNPTA Inclusion Cell Disease Leroy Disease ML Disorder, Type II ML II Mucolipidosis II N-Acetylglucosamine-1-Phosphotransferase Deficiency
Also known as: Disorders of Cornification
Also known as: Disorder of Cornification 8, Curth-Macklin Type DOC 8, Curth-Macklin Type
Also known as: ichthyosis simplex
Also known as: CHILD Naevus CHILD Nevus Congenital Hemidysplasia with Ichthyosis Erythroderma and Limb Defects Disorders of Cornification 16 DOC 16, Unilateral Hemidysplasia Type Unilateral Hemidysplasia Type Unilateral Ichthyosiform Erythroderma with Ipsilateral Malformations, Limb
Also known as: Comel-Netherton Syndrome Ichthyosis Linearis Circumflexa
Also known as: Placental Steroid Sulfatase Deficiency; STS Recessive X-linked Ichthyosis Steroid Sulfatase Deficiency Steroid Sulfatase Deficiency Disease; SSDD
Also known as: benign intracranial hypertension pseudotumor cerebri
Also known as: nodular nonsuppurative panniculitis Pfeiffer-Weber-Christian syndrome relapsing febrile nodular nonsuppurative panniculitis Weber Christian Disease (so-called)
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Also known as: cryptogenic fibrosing alveolitis idiopathic diffuse interstitial pulmonary fibrosis IPF
Also known as: IPH immune-mediated pulmonary hemosiderosis (ImPH) diffuse alveolar hemorrhage (DAH) diffuse pulmonary hemorrhage (DPH)
Also known as: idiopathic subglottic and tracheal stenosis iSGS ISS
Also known as: Berger's disease IgAN
Also known as: IMMAS SUZ12-related overgrowth disorder SUZ12-related overgrowth SUZ12-related neurodevelopmental disorder
Also known as: autoimmune thrombocytopenic purpura ITP idiopathic immune thrombocytopenia primary immune thrombocytopenia
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