Nervous System Diseases | Page 10

1250 diseases found in 13 pages

P Diseases

Pfeiffer Mayer syndrome Pfeiffer Palm Teller syndrome Pfeiffer-type cardiocranial syndrome PGM3-CDG PHACE syndrome Phosphoglycerate kinase deficiency Phosphoglycerate mutase deficiency Phosphoserine aminotransferase deficiency Photosensitive epilepsy Pitt-Hopkins-like syndrome Pitt-Hopkins syndrome Plasmacytoma Pleomorphic xanthoastrocytoma PMM2-CDG (CDG-Ia) POEMS syndrome Poliomyelitis POLR3-Related Leukodystrophy Polyarteritis nodosa Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome Pontine tegmental cap dysplasia Pontocerebellar hypoplasia Pontocerebellar hypoplasia type 1 Pontocerebellar hypoplasia type 2 Pontocerebellar hypoplasia type 3 Pontocerebellar hypoplasia type 4 Pontocerebellar hypoplasia type 5 Pontocerebellar hypoplasia type 6 Posterior column ataxia Posterior column ataxia with retinitis pigmentosa Postnatal progressive microcephaly, seizures, and brain atrophy Post Polio syndrome Potassium aggravated myotonia Potocki-Lupski syndrome PPM-X syndrome Prader-Willi habitus, osteopenia, and camptodactyly Primary amebic meningoencephalitis Primary angiitis of the central nervous system Primary basilar impression Primary carnitine deficiency Primary central nervous system lymphoma Primary Familial Brain Calcification Primary lateral sclerosis Primary melanoma of the central nervous system Primary orthostatic tremor Primary progressive aphasia Primrose syndrome Progressive bulbar palsy Progressive encephalomyelitis with rigidity and myoclonus Progressive external ophthalmoplegia, autosomal recessive 1 Progressive hemifacial atrophy Progressive non-fluent aphasia Prolidase deficiency Proteus syndrome Proud syndrome Pseudoaminopterin syndrome Pseudocholinesterase deficiency Pseudoneonatal adrenoleukodystrophy Pseudoprogeria syndrome Pseudotrisomy 13 syndrome Pseudoxanthoma elasticum Pterygium colli mental retardation digital anomalies Pudendal Neuralgia Pure autonomic failure Pyridoxal 5'-phosphate-dependent epilepsy Pyridoxine-dependent epilepsy Pyruvate dehydrogenase phosphatase deficiency

Q Diseases

Qazi Markouizos syndrome

R Diseases

Radiation induced brachial plexopathy Ramos Arroyo Clark syndrome Rapid-onset dystonia-parkinsonism Rasmussen encephalitis Reardon Wilson Cavanagh syndrome Reducing body myopathy Refsum disease Refsum disease, infantile form Renal dysplasia-limb defects syndrome Renier Gabreels Jasper syndrome Restless legs syndrome, susceptibility to, 1 Restless legs syndrome, susceptibility to, 2 Restless legs syndrome, susceptibility to, 3 Restless legs syndrome, susceptibility to, 4 Restless legs syndrome, susceptibility to, 5 Restless legs syndrome, susceptibility to, 6 Retinal arterial macroaneurysm with supravalvular pulmonic stenosis Retinal vasculopathy with cerebral leukodystrophy Rett syndrome Reversible cerebral vasoconstriction syndrome RFT1-CDG (CDG-In) Rhabdoid tumor Rhizomelic chondrodysplasia punctata type 1 Riboflavin transporter deficiency Richards-Rundle syndrome Richieri Costa Da Silva syndrome Rigid spine syndrome Ring chromosome 10 Ring chromosome 14 Ring chromosome 20 Rippling muscle disease RNAse T2-deficient leukoencephalopathy

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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