Abnormality of the endocrine system
Symptom Information:
Symptom ID: | HPO:0000818 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the endocrine system(HPO:0000818) MedDRA: |
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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) |