Potter's syndrome Disease Ontology Browser

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Disease Ontology Browser

Potter's syndrome (DOID:12594)
Alliance: disease page
Synonyms: Potter sequence; Potter syndrome
Alt IDs: ICD10CM:Q60.6, NCI:C40435, UMLS_CUI:C0178426
Definition: A renal agenesis characterized by the typical physical appearance and associated pulmonary hypoplasia of a newborn as a direct result of kidney failure, oligohydramnios and compression while in the uterus.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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