leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism https://github.com/monarch-initiative/mondo/issues/7693 https://github.com/monarch-initiative/mondo/issues/8351 https://www.malacards.org/card/hypomyelinating_leukodystrophy_7 https://www.malacards.org/card/leukodystrophy_hypomyelinating_7_with_or_without_oligodontia_and_or_hypogonadotropic_hypogonadism leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism NANDO:1200585 MONDO:0011897 4H syndrome leukoencephalopathy, hypomyelinating, with ataxia and delayed dentition GARD:0016948 SCTID:721846006 A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of childhood onset of progressive motor decline manifest as spasticity, ataxia, tremor, and cerebellar signs, as well as mild cognitive regression that has material basis in homozygous or compound heterozygous mutation in the POLR3A gene on chromosome 10q22. leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism DOID:0060794 HLD7 NANDO:2201297 hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism OMIM:607694 POLR3A-related disorder POLR3-related leukodystrophy