Adrenal hypoplasia

Symptom Information:

Symptom ID: HPO:0000835
Synonyms:
Adrenal gland hypoplasia [HPO:0000835]
Hypoplastic adrenal glands [HPO:0000835]
Small adrenal glands [HPO:0000835]
Adrenocortical insufficiency [Orphanet:41420]
Adrenal cortical hypofunction [Orphanet:41420]
Adrenal gland hypoplasia [OMIM:Adrenal gland hypoplasia]
Adrenal hypoplasia [OMIM:Adrenal hypoplasia]
Hypoplastic adrenal glands [OMIM:Hypoplastic adrenal glands]
Small adrenal glands [OMIM:Small adrenal glands]
Cortico-adrenal hypoplasia/insufficiency [Orphanet:41420]
Adrenocortical insufficiency (uncommon) [OMIM:Adrenocortical insufficiency (uncommon)]
Adrenal cortical hypofunctions [MedDRA:10001343]
Quality:
Cross references:
HPO:0008207 "Primary adrenal insufficiency" [Orphanet:41420]
HPO:0008182 "Adrenocortical hypoplasia" [Orphanet:41420]
HPO:0011735 "Adrenocorticotropin (ACTH) deficient adrenal insufficiency" [Orphanet:41420]
HPO:0000846 "Adrenal insufficiency" [Orphanet:41420]
Orphanet:41420 "Cortico-adrenal hypoplasia/insufficiency" [Orphanet:41420]
OMIM: "Adrenal gland hypoplasia" [OMIM:Adrenal gland hypoplasia]
OMIM: "Adrenal hypoplasia" [OMIM:Adrenal hypoplasia]
OMIM: "Hypoplastic adrenal glands" [OMIM:Hypoplastic adrenal glands]
OMIM: "Small adrenal glands" [OMIM:Small adrenal glands]
OMIM: "Adrenocortical insufficiency (uncommon)" [OMIM:Adrenocortical insufficiency (uncommon)]
UMLS:C0405580 "Adrenal cortical hypofunction" [Orphanet:41420]
Is a (Direct Parents):
MedDRA Adrenal gland disorders
HPO         Abnormality of adrenal morphology
Orphanet Abnormality of the adrenal glands
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the adrenal glands(HPO:0000834)
             Abnormality of adrenal morphology(HPO:0011732)
                Adrenal hypoplasia(HPO:0000835)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Adrenal gland disorders(MedDRA:10001353)
       Adrenal hypoplasia(HPO:0000835)
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
ADRENAL HYPOPLASIA, CONGENITAL (OMIM:300200)
Bifunctional enzyme deficiency (Orphanet:300)
CHILD syndrome (Orphanet:139)
Congenital isolated ACTH deficiency (Orphanet:199296)
Cytomegalic congenital adrenal hypoplasia (Orphanet:95702)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
HOLOPROSENCEPHALY 1 (OMIM:236100)
HOLOPROSENCEPHALY 2 (OMIM:157170)
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES (OMIM:613124)
HYPOADRENOCORTICISM, FAMILIAL (OMIM:240200)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
IMAGe syndrome (Orphanet:85173)
Kearns-Sayre syndrome (Orphanet:480)
Lethal restrictive dermopathy (Orphanet:1662)
MELAS (Orphanet:550)
MOVED TO 614732 (OMIM:300290)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Pallister-Hall syndrome (Orphanet:672)
Zellweger syndrome (Orphanet:912)