Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

11 matching diseasesClear search ×

VPS11-related autosomal recessive hypomyelinating leukodystrophy

VPS11-related autosomal recessive hypomyelinating leukoencephalopathy

ORPHA:466934

Autosomal recessive ACTN2-related distal myopathy

ORPHA:708129

Autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome

ORPHA:314572

Autosomal recessive spastic ataxia with leukoencephalopathy

ARSAL · Autosomal recessive spastic ataxia type 3

ORPHA:314603

C11ORF73-related autosomal recessive hypomyelinating leukodystrophy

C11ORF73-related autosomal recessive hypomyelinating leukoencephalopathy · Hypomyelinating leukodystrophy due to hikeshi deficiency

ORPHA:495844

Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy

Maeda syndrome · CARASIL

ORPHA:199354

Charcot-Marie-Tooth disease type 4E

Autosomal recessive congenital hypomyelinating neuropathy · CMT4E

ORPHA:99951

NKX6-2-related autosomal recessive hypomyelinating leukodystrophy

Autosomal recessive hypomyelinating leukodystrophy-progressive spastic ataxia · SPAX8

ORPHA:527497

Progressive cavitating leukoencephalopathy

ORPHA:139447

PYCR2-related microcephaly-progressive leukoencephalopathy

ORPHA:481152

RARS-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:438114