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DO Term : Seckel syndrome 1 [DOID:0070007] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23.

synonyms:
microcephalic primordial dwarfism I,
MESH:C537533,
SCKL1,
210600,
OMIM:210600

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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