HSD17B7

hydroxysteroid 17-beta dehydrogenase 7
OMIM: 606756, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red HSD17B7 in Mendeliome


Version 2.268

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Sensorineural hearing loss disorder, MONDO:0020678

Red HSD17B7 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 2.4

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Sensorineural hearing loss disorder, MONDO:0020678