Abnormality of the endocrine system

Symptom Information:

Symptom ID: HPO:0000818
Synonyms:
Endocrine system disease [HPO:0000818]
Endocrine anomaly [Orphanet:41000]
Anomalies of the endocrine glands [Orphanet:41000]
Quality:
Cross references:
Orphanet:41000 "Anomalies of the endocrine glands" [Orphanet:41000]
Is a (Direct Parents):
HPO         Phenotypic abnormality
HPO         Abnormality of the pineal gland
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
MedDRA:
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency (Orphanet:753)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Acromegaly (Orphanet:963)
Biemond syndrome type 2 (Orphanet:141333)
CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION (OMIM:304200)
Central congenital hypothyroidism (Orphanet:226298)
Chronic mucocutaneous candidiasis (Orphanet:1334)
ECTODERMAL DYSPLASIA WITH ADRENAL CYST (OMIM:129550)
Hemochromatosis type 2 (Orphanet:79230)
Laron syndrome (Orphanet:633)
Leprechaunism (Orphanet:508)
MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 1 (OMIM:300488)
MERRF (Orphanet:551)
Multiple endocrine neoplasia type 1 (Orphanet:652)
Neurofibromatosis type 1 (Orphanet:636)
PLATELET GLYCOPROTEIN IV DEFICIENCY (OMIM:608404)
PYGMY (OMIM:265850)
Pearson syndrome (Orphanet:699)
RENIN (OMIM:179820)
RENIN-BINDING PROTEIN (OMIM:312420)
Scalp-ear-nipple syndrome (Orphanet:2036)
Steinert myotonic dystrophy (Orphanet:273)
THIOUREA TASTINGPHENYLTHIOCARBAMIDE TASTING, INCLUDED (OMIM:171200)
THYMIC APLASIA WITH FETAL DEATH (OMIM:274210)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)