Disease #01748

Official abbreviation CPHD-3
Name hormone deficiency, pituitary, combined, type 3 (CPHD-3)
OMIM ID 221750
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene LHX3
Associated tissues -
Disease features autosomal recessive
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

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Consanguinity     

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Age/Death     

VIP     

Data_av     

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Disease     

Phenotype details     

Genes screened

Variants in genes

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Owner     
00163928 - - - M ? Italy - - 0 - - CPHD-3 - LHX3 LHX3 1 1 Pauline Romanet
00163929 - - - F yes Iran - - 0 - - CPHD-3 - LHX3 LHX3 1 1 Pauline Romanet
00163930 - - - M ? Argentina - - 0 - - CPHD-3 - LHX3 LHX3 1 1 Pauline Romanet
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