Abnormality of the hypothalamus-pituitary axis
Symptom Information:
Symptom ID: | HPO:0000864 | ||||||||||||||||||
Synonyms: |
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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) Abnormality of the hypothalamus-pituitary axis(HPO:0000864) MedDRA: Endocrine disorders(MedDRA:10014698) Hypothalamus and pituitary gland disorders(MedDRA:10021112) Hypothalamic and pituitary disorders NEC(MedDRA:10021109) Abnormality of the hypothalamus-pituitary axis(HPO:0000864) |
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Database Frequency: | 23 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
14q22q23 microdeletion syndrome | (Orphanet:264200) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
Aniridia | (Orphanet:77) |
Axenfeld-Rieger syndrome | (Orphanet:782) |
Brain malformation - congenital heart disease - postaxial polydactyly | (Orphanet:75389) |
CHARGE syndrome | (Orphanet:138) |
Cerebellar ataxia - hypogonadism | (Orphanet:1173) |
Diencephalic syndrome | (Orphanet:1672) |
Fanconi anemia | (Orphanet:84) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Joubert syndrome with renal defect | (Orphanet:220497) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Pallister-Hall syndrome | (Orphanet:672) |
Pituitary stalk interruption syndrome | (Orphanet:95496) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
Septo-optic dysplasia | (Orphanet:3157) |