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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Hallermann's Syndrome

hallermann's syndrome

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Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

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Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Hallermann's Syndrome
Standard Disease Name
hallermann's syndrome
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D006210
OMIM ID
234100
UMLS ID
C0018522
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A very rare syndrome characterized by multiple congenital abnormalities including abnormally shaped head, mandibular hypoplasia, parrot nose, bilateral congenital cataracts, microphthalmia, dwarfism and hypotrichosis.|MSH2017_2016_08_12:An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed)|JABL99:A bulging skull with brachycephaly, beaked nose, cataracts, microphthalmia and receding chin giving the face its peculiar bird-like appearance. Associated defects include hypotrichosis, short stature, occasional mental deficiency and skeletal, hepatic, muscular, and renal anomalies.