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"

54 matching diseasesClear search ×

Kabuki syndrome

Kabuki make-up syndrome · Niikawa-Kuroki syndrome

ORPHA:2322

3M syndrome

3-M syndrome · Yakut short stature syndrome

ORPHA:2616

46,XX testicular difference of sex development

46,XX testicular DSD · De la Chapelle syndrome

ORPHA:393

Autosomal recessive spastic paraplegia type 21

Mast syndrome · SPG21

ORPHA:101001

Cataract-intellectual disability-hypogonadism syndrome

Martsolf syndrome

ORPHA:1387

Catel-Manzke syndrome

Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome · Index finger anomaly-Pierre Robin syndrome

ORPHA:1388

Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy

Maeda syndrome · CARASIL

ORPHA:199354

Colobomatous macrophthalmia-microcornea syndrome

MACOM syndrome

ORPHA:468672

Congenital insensitivity to pain syndrome, Marsili type

Marsili syndrome

ORPHA:653728

Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

Cardiogenital syndrome · Malouf syndrome

ORPHA:2229

Epidermolysis bullosa simplex with anodontia/hypodontia

Kallin syndrome · EBS with anodontia/hypodontia

ORPHA:2325

Familial atypical multiple mole melanoma syndrome

B-K mole syndrome · FAMM-PC syndrome

ORPHA:404560

Fibrodysplasia ossificans progressiva

FOP · Myositis ossificans progressiva

ORPHA:337

Fibrous dysplasia/McCune-Albright syndrome

Fibrous dysplasia/McCune-Albright spectrum · FD/MAS spectrum

ORPHA:595216

Hyperphosphatasia-intellectual disability syndrome

Mabry syndrome

ORPHA:247262

Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome

MOMES syndrome

ORPHA:397973

Kahrizi syndrome

Intellectual disability, Kahrizi type · Intellectual disability-cataract-coloboma-kyphosis syndrome

ORPHA:168972

Kallmann syndrome

Congenital hypogonadotropic hypogonadism with anosmia · Olfacto-genital pathological sequence

ORPHA:478

KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome

KAT6A syndrome · Arboleda-Tham syndrome

ORPHA:457193

KBG syndrome

Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome · ANKRD11-related disorder

ORPHA:2332

KID syndrome

KID/HID syndrome · Keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome

ORPHA:477

Maffucci syndrome

Multiple Enchondromatosis, Maffucci Type · Multiple Enchondromatosis type II

ORPHA:163634

MAGIC syndrome

Mouth and genital ulcers-inflamed cartilage syndrome

ORPHA:324972

Majeed syndrome

Chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome

ORPHA:77297

Malpuech syndrome

3MC3 syndrome · Malpuech facial clefting syndrome

ORPHA:2453

Mammary-digital-nail syndrome

MDN syndrome · Onycho-digito-mammary syndrome

ORPHA:238744

Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome

MDPL syndrome · MDP syndrome

ORPHA:363649

Mandibulofacial dysostosis-microcephaly syndrome

MFDM syndrome · Mandibulofacial dysostosis, Guion-Almeida type

ORPHA:79113

Marfan syndrome

MFS

ORPHA:558

Marshall syndrome

ORPHA:560

MASA syndrome

Intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome

ORPHA:2466

MASS syndrome

Mitral valve-aorta-skeleton-skin syndrome

ORPHA:99715

Mayer-Rokitansky-Küster-Hauser syndrome

MRKH syndrome · Rokitansky syndrome

ORPHA:3109

Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome

MPPH syndrome

ORPHA:83473

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

Melorheostosis with osteopoikilosis

MSBD syndrome · Mixed sclerosing bone dystrophy

ORPHA:1879

MEND syndrome

Male EBP disorder with neurological defects

ORPHA:401973

Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome

MPPC syndrome

ORPHA:231736

Microphthalmia with linear skin defects syndrome

MCOPS7 · MIDAS syndrome

ORPHA:2556

Microphthalmia-brain atrophy syndrome

MCOPS10 · MOBA syndrome

ORPHA:77299

MMEP syndrome

MCOPS8 · Microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome

ORPHA:3434

MOMO syndrome

Macrocephaly-obesity-intellectual disability-ocular abnormalities syndrome · Macrosomia-obesity-macrocephaly-ocular abnormalities syndrome

ORPHA:2563

MORM syndrome

Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome

ORPHA:75858

MRCS syndrome

Microcornea-rod-cone dystrophy-cataract-posterior staphyloma syndrome

ORPHA:263347

Muenke syndrome

ORPHA:53271

Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

MARCH syndrome

ORPHA:500135

Muscle-eye-brain disease

MEB syndrome · Muscle-eye-brain syndrome

ORPHA:588

Neurogenic scapuloperoneal syndrome, Kaeser type

Kaeser syndrome · Stark-Kaeser syndrome

ORPHA:85146