Primary hypothyroidism

Symptom Information:

Symptom ID: HPO:0000832
Synonyms:
Primary hypothyroidism [OMIM:Primary hypothyroidism]
Primary hypothyroidism (reported in 2 patients) [OMIM:Primary hypothyroidism (reported in 2 patients)]
Primary hypothyroidism [MedDRA:10036697]
Quality:
Cross references:
OMIM: "Primary hypothyroidism" [OMIM:Primary hypothyroidism]
OMIM: "Primary hypothyroidism (reported in 2 patients)" [OMIM:Primary hypothyroidism (reported in 2 patients)]
Is a (Direct Parents):
MedDRA Thyroid hypofunction disorders
HPO         Hypothyroidism
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)
                   Primary hypothyroidism(HPO:0000832)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Thyroid gland disorders(MedDRA:10043739)
       Thyroid hypofunction disorders(MedDRA:10043741)
          Primary hypothyroidism(HPO:0000832)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)