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"

15 matching diseasesClear search ×

Male infertility due to large-headed multiflagellar polyploid spermatozoa

Male infertility due to macrozoospermia · Macrocephalic sperm head syndrome

ORPHA:137893

Chromosome Y microdeletion syndrome

Male infertility due to chromosome Y microdeletion · Microdeletion of the AZF region on the Y chromosome

ORPHA:1646

Female infertility due to oocyte meiotic arrest

ORPHA:488191

Male infertility due to acephalic spermatozoa

Acephalic spermatozoa syndrome

ORPHA:529970

Male infertility due to globozoospermia

Round-headed sperm syndrome · Male infertility due to round-headed spermatozoa

ORPHA:171709

Male infertility due to gonadal dysgenesis or sperm disorder

Male infertility due to testicular dysgenesis or sperm disorder

ORPHA:399764

Male infertility due to NANOS1 mutation

ORPHA:352613

Male infertility due to obstructive azoospermia of genetic origin

Male infertility due to impaired sperm transport of genetic origin

ORPHA:399998

Male infertility due to sperm disorder

ORPHA:399771

Male infertility due to sperm motility disorder

Male infertility due to asthenozoospermia

ORPHA:399813

Male infertility with azoospermia or oligozoospermia due to single gene mutation

ORPHA:399805

Male infertility with teratozoospermia due to single gene mutation

ORPHA:399808

Non-syndromic male infertility due to sperm motility disorder

Non-syndromic male infertility due asthenozoospermia

ORPHA:276234

Rare male infertility

ORPHA:98048

Rare male infertility due to adrenal disorder

ORPHA:399584