Phenotypes for disease #01748 (CPHD3 (hormone deficiency, pituitary, combined, type 3), OMIM:221750)

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

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000129038 neonatal panhypopituitarism, ACTH deficiency, TSH deficiency, GH deficiency; retinal dystrophy, low-set ears; MRI brain cystic anterior pituitary, corpus callosum digenesis neonatal panhypopituitarism CPHD3 Familial, autosomal recessive 02y - - - - Pauline Romanet 00163929
0000129039 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 neonatal panhypopituitarism - Unknown 03y - - - - Pauline Romanet 00163930
0000129040 neonatal panhypopituitarism, micropenis, ACTH deficiency, TSH deficiency, GH deficiency; MRI brain normal, no malformations; carrier mother 40y-normal pituitary evaluation - - Unknown - 02y - - - Pauline Romanet 00163928
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