Disease #01748 (CPHD3 (hormone deficiency, pituitary, combined, type 3), OMIM:221750)

Official abbreviation CPHD3
Name hormone deficiency, pituitary, combined, type 3
OMIM ID 221750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene LHX3
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-12-22 16:34:37 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00163928 FamAPatA PubMed: Jullien 2019, Journal: Jullien 2019 2-generation family, 1 affected, unaffected carrier mother M ? Italy - - - - - CPHD3 neonatal panhypopituitarism, micropenis, ACTH deficiency, TSH deficiency, GH deficiency; MRI brain normal, no malformations; carrier mother 40y-normal pituitary evaluation LHX3 LHX3 3 1 Pauline Romanet
00163929 FamBPatB PubMed: Jullien 2019, Journal: Jullien 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents F yes Iran - - - - - CPHD3 neonatal panhypopituitarism, ACTH deficiency, TSH deficiency, GH deficiency; retinal dystrophy, low-set ears; MRI brain cystic anterior pituitary, corpus callosum digenesis LHX3 LHX3 3 1 Pauline Romanet
00163930 PatC PubMed: Jullien 2019, Journal: Jullien 2019 - M ? Argentina - - - - - CPHD3 neonatal panhypopituitarism, ACTH deficiency, microcephaly, micropenis; birth no hypoglycemia; 2y-GH deficiency; 3y-TSH deficiency; MRI brain anterior pituitary hypoplasia, thin pituitary stalk, non-visualized posterior pituitary LHX3 LHX3 1 1 Pauline Romanet
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