Pituitary hypothyroidism

Symptom Information:

Symptom ID: HPO:0008245
Synonyms:
Secondary hypothyroidism [HPO:0008245]
Thyroid stimulating hormone deficiency [HPO:0008245]
Thyrotropin deficiency [HPO:0008245]
TSH deficient hypothyroidism [HPO:0008245]
Thyroid stimulating hormone deficiency [OMIM:Thyroid stimulating hormone deficiency]
Hypothyroidism, secondary [OMIM:Hypothyroidism, secondary]
Secondary hypothyroidism [MedDRA:10039840]
Quality:
Cross references:
OMIM: "Thyroid stimulating hormone deficiency" [OMIM:Thyroid stimulating hormone deficiency]
OMIM: "Hypothyroidism, secondary" [OMIM:Hypothyroidism, secondary]
Is a (Direct Parents):
HPO         Anterior hypopituitarism
HPO         Central hypothyroidism
MedDRA Thyroid hypofunction disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the thyroid gland(HPO:0000820)
             Abnormality of thyroid physiology(HPO:0002926)
                Hypothyroidism(HPO:0000821)
                   Central hypothyroidism(HPO:0011787)
                      Pituitary hypothyroidism(HPO:0008245)
          Abnormality of the hypothalamus-pituitary axis(HPO:0000864)
             Abnormality of the pituitary gland(HPO:0012503)
                Abnormality of the anterior pituitary(HPO:0011747)
                   Anterior hypopituitarism(HPO:0000830)
                      Pituitary hypothyroidism(HPO:0008245)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Thyroid gland disorders(MedDRA:10043739)
       Thyroid hypofunction disorders(MedDRA:10043741)
          Pituitary hypothyroidism(HPO:0008245)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Microphthalmia with brain and digit anomalies (Orphanet:139471)
Obesity due to leptin receptor gene deficiency (Orphanet:179494)
RHYNS syndrome (Orphanet:140976)
WEBB-DATTANI SYNDROME (OMIM:615926)