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Diseases

Wittwer Syndrome

wittwer syndrome

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

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

Core Information

Disease Name
Wittwer Syndrome
Standard Disease Name
wittwer syndrome
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
C536737
OMIM ID
194190
UMLS ID
C0796202
HPO ID
No data

Description and Extensions

Description
JABL99:Mental retardation with multiple congenital abnormalities consisting of craniofacial anomalies, delayed development, skeletal anomalies, urogenital anomalies, and deformed hands.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
FGFR3
fibroblast growth factor receptor 3
fibroblast growth factor receptor 3
02
LETM1
leucine zipper and EF-hand containing transmembrane protein 1
leucine zipper and EF-hand containing transmembrane protein 1
05
NELFA
negative elongation factor complex member A
negative elongation factor complex member A
06
NSD2
nuclear receptor binding SET domain protein 2
nuclear receptor binding SET domain protein 2