CHILD syndrome

Summary
Synonym
  • CHILD nevus
  • congenital hemidysplasia with ichthyosiform nevus and limbs defects
Definition
A syndrome characterized by congenital hemidysplasia, ichythyosiform erythrodema, and limb defects that has_material_basis_in heterozygous mutation in the NSDHL gene on chromosome Xq28.
Super Class
X-linked dominant disease syndrome
External Links
Disease Ontology
DOID:0111822
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
50814 NSDHL NAD(P) dependent steroid dehydrogenase-like
The Human Phenotype Ontology
Displaying entries 1 - 10 of 48 in total
HPO ID HPO Term
HP:0000122 Unilateral renal agenesis
HP:0000126 Hydronephrosis
HP:0000204 Cleft upper lip
HP:0000347 Micrognathia
HP:0000365 Hearing impairment
HP:0000773 Short ribs
HP:0000835 Adrenal hypoplasia
HP:0000882 Hypoplastic scapulae
HP:0000894 Short clavicles
HP:0000954 Single transverse palmar crease
Displaying 1 entry
Gene ID Gene Symbol Description
50814 NSDHL NAD(P) dependent steroid dehydrogenase-like

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024