Adrenal hypoplasia
Symptom Information:
Symptom ID: | HPO:0000835 | ||||||||||||
Synonyms: |
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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) 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) |
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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) |