Abnormality of the hypothalamus-pituitary axis

Symptom Information:

Symptom ID: HPO:0000864
Synonyms:
Hypothalamic hypophyseal axis anomaly [Orphanet:41030]
Disorder of pituitary gland (disorder) [Orphanet:41030]
Pituitary Diseases [Orphanet:41030]
Hypothalamic-hypophyseal axis anomalies/hypothalamus/pituitary anomalies [Orphanet:41030]
Pituitary disorder [Orphanet:41030]
Hypothalamo-pituitary disorder [MedDRA:10021111]
Disorders of the pituitary gland and its hypothalamic control [MedDRA:10021111]
Disorders of the pituitary gland and its hypothalmic control [MedDRA:10021111]
Iatrogenic pituitary disorders [MedDRA:10021111]
Other anterior pituitary disorders [MedDRA:10021111]
Other disorders of neurohypophysis [MedDRA:10021111]
Other disorders of the pituitary and other syndromes of diencephalo-hypophyseal origin [MedDRA:10021111]
Other disorders of the pituitary and other syndromes of diencephalohypophyseal origin [MedDRA:10021111]
Pituitary disorder NOS [MedDRA:10021111]
Unspecified disorder of the pituitary gland and its hypothalamic control [MedDRA:10021111]
Unspecified disorder of the pituitary gland and its hypothalmic control [MedDRA:10021111]
Pituitary disorder [MedDRA:10021111]
Hypothalamic disorder [MedDRA:10021111]
Quality:
Cross references:
Orphanet:41030 "Hypothalamic-hypophyseal axis anomalies/hypothalamus/pituitary anomalies" [Orphanet:41030]
UMLS:C0032002 "Pituitary Diseases" [Orphanet:41030]
Is a (Direct Parents):
HPO         Abnormality of the endocrine system
Orphanet Abnormality of the endocrine system
MedDRA Hypothalamic and pituitary disorders NEC
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)
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)