MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Trichodental syndrome

ORPHA:3351Malf.
Autosomal dominant

Trichodermodysplasia-dental alterations syndrome

ORPHA:3353Malf.

Trichodysplasia-amelogenesis imperfecta syndrome

ORPHA:79129Malf.
X-linked recessive

Trichodysplasia-xeroderma syndrome

ORPHA:3361Malf.

Trichofolliculoma

ORPHA:864Kr.
Not applicable

Trichohepatoenteric syndrome

ORPHA:84064Kr.
Autosomal recessive

Trichomegaly-retina pigmentary degeneration-dwarfism syndrome

ORPHA:3363Malf.
Autosomal recessive

Trichoodontoonychial dysplasia

ORPHA:3355Malf.
Autosomal recessive

Trichorhinophalangeal syndrome type 1

ORPHA:77258Malf.
Autosomal dominant

Trichorhinophalangeal syndrome type 2

ORPHA:502Malf.
Autosomal dominant

Trichothiodystrophy

ORPHA:33364Kr.
Autosomal recessive, X-linked recessive

Tricuspid atresia

ORPHA:1209Morph.
Not applicable

Trigeminal neuralgia

ORPHA:221091Kr.
Not applicable

Trigeminal trophic syndrome

ORPHA:664901Kr.

Triglyceride deposit cardiomyovasculopathy

ORPHA:692305Kr.
Autosomal recessive, Unknown

Trigonocephaly-bifid nose-acral anomalies syndrome

ORPHA:3368Malf.
Unknown

Trigonocephaly-broad thumbs syndrome

ORPHA:3365Malf.
Autosomal dominant

Trigonocephaly-short stature-developmental delay syndrome

ORPHA:3369Malf.
Unknown

Triose phosphate-isomerase deficiency

ORPHA:868Kr.
Autosomal recessive

Triphalangeal thumbs-brachyectrodactyly syndrome

ORPHA:2947Malf.
Autosomal dominant

Triple A syndrome

ORPHA:869Kr.
Autosomal recessive

Triploidy syndrome

ORPHA:3376Malf.
Not applicable, Unknown

Trismus-pseudocamptodactyly syndrome

ORPHA:3377Malf.
Autosomal dominant

Trisomy 10p syndrome

ORPHA:171929Malf.