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DO Term : Potter's syndrome [DOID:12594] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
SNOMEDCT_US_2023_03_01:41962002,
Potter sequence,
ICD10CM:Q60.6,
Potter syndrome,
UMLS_CUI:C0178426,
NCI:C40435,
GARD:4462

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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