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MCID: ART047
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Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia malady |
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Sources: 22MalaCards See all sources Export this MalaCard |
MalaCards: Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia, is also known as arthrogryposis multiplex congenita, pulmonary hypoplasia, cryptorchidism, and unusual ophthalmological findings. An important gene associated with Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia is RAPSN (receptor-associated protein of the synapse).
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Aliases & Descriptions for Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
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Sources: 30NIH Rare Diseases, 43UMLS See all sources |
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Sources: 4CenterWatch, 29NIH Clinical Center, 5ClinicalTrials See all sources |
Approved drugs:Search CenterWatch for arthrogryposis multiplex congenita pulmonary hypoplasia Drug clinical trials:Search ClinicalTrials for arthrogryposis multiplex congenita pulmonary hypoplasia Search NIH Clinical Center for arthrogryposis multiplex congenita pulmonary hypoplasia Search CenterWatch for arthrogryposis multiplex congenita pulmonary hypoplasia |
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Phenotypes for genes affiliated with Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
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Publications for genes affiliated with Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
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Expression for genes affiliated with Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
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Sources: 1BioGPS See all sources |
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Pathways for genes affiliated with Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
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Compounds for genes affiliated with Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
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GO Terms for genes affiliated with Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
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