Online Directory

Section 1A

Disorders MIM Genes MIM Specialties Commissioning
Rapp-Hodgkin Syndrome; RHS 129400
tumor protein p63; TP63 603273
  • Clinical Genetics
  • Dental Surgery, Paediatric
  • Dermatology, Paediatric
Renal Cell Carcinoma, Papillary, 1; RCCP1 605074
MET proto-oncogene, receptor tyrosine kinase; MET 164860
  • Nephrology, Adult
  • Oncology, Adult
Renal Cysts And Diabetes Syndrome; RCAD 137920
HNF1 homeobox B; HNF1B 189907
Renal Tubular Acidosis, Distal, Autosomal Dominant 179800
solute carrier family 4 member 1 (Diego blood group); SLC4A1 109270
  • Nephrology, Adult
Renal Tubular Acidosis, Distal, Autosomal Recessive; RTADR 602722
ATPase H+ transporting V0 subunit A4; ATP6V0A4 605239
  • Clinical Genetics
  • Nephrology, Adult
  • Nephrology, Paediatric
Renal Tubular Acidosis, Distal, With Progressive Nerve Deafness 267300
ATPase H+ transporting V1 subunit B1; ATP6V1B1 192132
  • Clinical Genetics
  • Nephrology, Adult
  • Nephrology, Paediatric
Retinitis Pigmentosa 1; RP1 180100
RP1, axonemal microtubule associated; RP1 603937
  • Clinical Genetics
  • Ophthalmology, Adult
Retinitis Pigmentosa 10; RP10 180105
inosine monophosphate dehydrogenase 1; IMPDH1 146690
  • Clinical Genetics
  • Ophthalmology, Adult
Retinitis Pigmentosa 11; RP11 600138
pre-mRNA processing factor 31; PRPF31 606419
  • Clinical Genetics
  • Ophthalmology, Adult
Retinitis Pigmentosa 13; RP13 600059
pre-mRNA processing factor 8; PRPF8 607300
  • Clinical Genetics
  • Ophthalmology, Adult

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