Submission Details

Submitter:

Classification:
Supportive
GENCC:100009
Gene:
Disease:
short stature-optic atrophy-Pelger-HuC+t anomaly syndrome
Orphanet:391677
Mode Of Inheritance:
Autosomal recessive
Evaluated Date:
09/14/2021
PubMed IDs:
20577004
Assertion Criteria:
Submitter Submitted Date:
09/14/2021

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